Pharmaceutical Jurisprudence and Ethics A.

device
(Red PACOP) B. drugs
C. cosmetics
D. poison
1.) The following persons shall be liable for E.Biologicproducts
violation(s) of RA 8203 except:
A. the manufacturer of the counterfeit drugs 8.) It refers to the approved clinical use of the product
B. importer or agents of counterfeit drugs based on substantial and scientifically supported
C. the registered pharmacist who has actual evidence of the safety and efficacy of the drug in the
or constructive knowledge about the given dosage form:
counterfeit drugs A. pharmacologic category
D. the registered pharmacist who has no B. indication
actual or constructive knowledge about the C. dosage formulation
counterfeit drugs D. dosage form
E. none E. expiry date

2.) Which of the following statement is/are true for 9.) A drug which has been used for at least five (5)
detail man? years and involving at least 5,000 patients:
A. an initial fee of twenty pesos is needed A. investigational drugs
upon registration B. established drugs
B. he shall be, preferably a graduate of a C. new drugs
College of Pharmacy D. tried & tested drug
C. to be employed, he needs to possess the E. Innovation of the tried and tested drug and
necessary credentials issued by the PRC established drug
D. only A and B
E. All of the above 10.) In Human Studies- Clinical Pharmacology III:
A. Controlled Clinical Trials
3.) This order gives comprehensive guidelines on the B. Safety and Efficacy
registration of pharmaceutical products to be C. Tolerance and Safety
consistent with RA 6675: D. Post Marketing Surveillance
A. AO 220 E. Provisional Monitored Release
B. AO 42
C. AO 67 11.) It is a drug which contains no amount of, or a
D. AO 90 different active ingredient, or less than 80% of the
E. AO 56 active ingredient it purports to possess, as
distinguished from an adulterated drug including
4.) This order defines rules & regulations governing reduction or loss of efficacy due to expiration:
the registration and sale of herbals and/or traditional A. Counterfeit drug
drugs to ensure their quality and safety: B. New drug
A. AO 220 C. Investigational drug
B.AO 42 D. Tried & Tested drug
C. AO 56 E. Ethical drug
D. AO 67
E. AO 90 12.) Any person whether related to the senior citizen
or not who takes care of him/her as dependent:
5.) Any person who shall violate RA 6675, sec 12 (a) A. head of the family
for the first conviction shall suffer the penalty of B. benefactor
reprimand which shall be officially recorded in the C. beneficiary
appropriate books of the: D. protector
A. PRC E. dependent
B.BOP
C. DDB 13.) It is a license issued by the Director General of
D. CPE the Intellectual Property Office (IPO) to exploit a
E. PPhA patented invention without the permission of the
patent holder either by manufacture or through
6.) They ensure the provision of safe, effective and parallel importation:
quality drugs, for improved patient care and quality of A. Certificate of Product Registration
life by helping individuals protect themselves against B. Compulsory license
diseases, maintain good health and make the best C. batch certificate
use of their medication. D. PRC license
A. teachers E. NOTA
B. pharmacist
C. medical technologist 14.) It refers to pharmaceutically equivalent or
D. veterinarian pharmaceutically alternative products that may or may
E. pharmacy technician not be therapeutically equivalent:
A. multisource pharmaceutical products
7.) An article intended to be rubbed, poured, B. multi-pharmaceutical products
sprinkled, or sprayed on, introduced into, or otherwise C. source pharmaceutical products
applied to the human body or any part thereof for D. generic products
cleansing, beautifying, promoting attractiveness, or E. pharmaceutical products
altering appearance:
15.) Any person who sells, trades, administers, A. 5291
dispenses, delivers, or gives away to another, on any B. 6675
term whatsoever, or distributes dispatches in transit or C. 3720
transport dangerous drugs or who act as a broker in D. 8203
any such transactions: E. 5921
A. practitioner 24.) The Generics Act of 1988 is known as R.A:
B. coddler A. 5921
C. protector B. 6675
D. pusher C. 3720
E. drug syndicate D. 8203
E. 8293
16) If the entire batch of product is marketed under
one company, only the lot number needs to be 25.) The Intellectual Property Code of the Philippines
indicated: in known as R.A:
A. the statement is incorrect A. 7432
B. the statement is correct B. 7581
C. both the batch and the lot number should C. 8293
be indicated D. 7394
D. only the registration number is needed E. 7581
E. None of the above
26.) The Special Law on Counterfeit Drug is known as
17.) Dangerous drug prescriptions shall be retained R.A:
by the pharmacist for a period of: A. 5921
A. 3 years B. 6675
B. 2 years C. 3720
C. 4 years D.8203
D. 5 years E. 8293
E. 1 year
27.) The Comprehensive Dangerous Drug Act of 2002
18.) Drug Registration of Herbal and/or Traditional is known as R.A:
Drugs (Local & Imported): A. 9257
A. AO 63 B. 9502
B. AO 62 C. 9165
C. AO 42 D. 9205
D. AO 55 E. 9711
E. AO 56
28.) Revised Rules and Regulations to Implement
19.) Revised Rules and Regulations to implement Prescribing Requirements under the Generic Act of
Prescribing Requirements under the Generics Act of 1988:
1988: A. AO 63
A. AO 63 B. AO 67
B. AO 62 C. AO 42
C. AO 42 D. AO 55
D. AO 55 E. AO 62
E. AO 67
29.) Revised Rules and Regulations to Implement
20.) Revised Regulations for the licensing of Drug Dispensing Requirements under the Generic Act of
Establishments and Outlets: 1988:
A. AO 42 A. AO 63
B. AO 90 B. AO 62
C. AO 64 C. AO 42
D. AO 56 D. AO 55
E. AO 55 E. AO 56

21.) The Universally Accessible Cheaper and Quality 30.) Revised Rules and Regulations on Registration
Medicines Act of 2008 is known as R.A: of Pharmaceutical Products:
A. 9257 A. AO 67
B. 9502 B. AO 90
C. 9165 C. AO 64
D. 9205 D. AO 56
E. 9527 E. AO 42

22.) The Expanded Senior Citizens Act of 2003 is 31.) The principal Display Panel comprises ____% of
known as R.A: the total surface of the container:
A. 9527 A. 10
B. 9502 B. 40
C. 9257 C. 80
D. 9165 D. 95
E. 9205 E. 85

23.) The Pharmacy Law is known as R.A:

32.) The test for alcohol content for registration of D. Director of BFAD
herbal and/of traditional drugs should not be more E. Director of FDA
than ____%:
A. 10 40.) According to A.O 55, under the formulation,
B. 40 drugs with multiple components must be arranged in
C. 80 order of:
D. 95 A. decreasing pharmacologic activity
E. 15 B. increasing pharmacologic activity
C. alphabetically
33.) Amount of marijuana subject to life imprisonment D. according to use
to death and a fine ranging from 500,000 pesos to E. according to pharmacologic category
10M pesos:
A. 500g 41.) Authorized to establish and initiate a price
B. 10g monitoring and regulation system for drugs and
C. 50g medicines:
D. 40g A. Secretary of the FDA
E. 30g B. Secretary of the DTI
C. Secretary of the DENR
34.) Amount of heroin subject to life imprisonment to D. Both B and C
death and a fine ranging from 500,000 pesos to 10M E. Secretary of the DOH
pesos:
A. 500g 42.) For products containing 3 or more active
B. 10g ingredients, the official name for the combination shall
C. 50g be designated by:
D. 40g A. DOST
E. 30g B. DTI
C. DOH
35.) If the seized drug was found to be counterfeit, the D. BFAD
business establishment must be directed for E. FDA
preventive closure for a period of:
A. 10 days 43.) The one responsible in ensuring that all drugs
B. 15 days authorized for marketing in the country conform to
C. 60 days international standards for the content, purity and
D. 30 days quality of pharmaceutical products as established in
E.25 days the International Pharmacopeia is:
A. BFAD
36.) The confiscated or seized dangerous drugs, plant B. DTI
sources, controlled precursor and essential chemicals C. DOH
shall be submitted to PDEA Forensic Laboratory for a D. DOST
quantitative examination within: E. DENR
A. 12 hours
B. 48 hours 44.) The following must be displayed conspicuously
C. 24 hours inside the drug outlet:
D. 16 hours A. certificate of product registration
E. 6 hours B. diploma of the pharmacist-in-charge
C. certificate of registration of the pharmacy
37.) The decision of the Board of Pharmacy in D. certificate of registration of the pharmacy
administrative cases involving a pharmacist becomes technician-in-charge
final and executor after the lapse of: E. certificate of registration of the pharmacist-
A. 15 days in-charge
B. 60 days
C. 30 days 45.) Grounds for suspension of LTO of Drug
D. NMT 6 months from notice to respondent Establishment:
E. 10 days A. lapses in record keeping of invoices
B. sale of antibiotics without batch certification
38.) Drug test certificates issued by accredited drug C. selling of misbranded drugs
testing centers shall be valid for _____ period from D. serious repeated or rampant violation of
the date of issued: existing laws, rules & regulations
A. 2 years E. lapses in record keeping of CPR
B. 1 month
C. 3 months 46.) Requirements for product registration, except:
D. 6 months A. prescription
E. 1 year B. brand identification
C. prescribing & dispensing regulations
39.) Responsible in granting a license to exploit a applicable
patented invention, even without the agreement of the D. available scientific evidence
patent owner, in favor of any person who has shown E. price
the capability to exploit the invention:
A. Director General of the IPO 47.) The source or circumstances of drug production
B. Director General of PDEA is/are:
C. Director of NBI A. imported as finished
 B. locally manufactured from local materials B. antibiotics
C. locally manufactured from imported C. new drugs
materials D. new veterinary drugs
D. all of the above E. biologic products
E. none of the above
56.) The concentration of known active drug
48.) In a drug establishment, personnel responsible substance in formulation:
for directing the manufacture and control must: A. strength
A. be inadequate of number B. net content
B. graduate of any 4 year course C. component
C. has capabilities to commensurate with D. stability
assigned function E. expiry date
D. experience is not necessary
E. all of the above 57.) Articles (other than food) intended to affect the
structure or any function of the body of man and
49.) Heavy metals to be tested in the herbal and/or recognized in the Philippine National Formulary:
traditional drugs EXCEPT: A. medicinal plants
A. Hg B. traditional drugs
B. Pb C. herbal drugs
C. As D. Both B and C
D. Cu E. none of the above
E. Mercury
58.) It refers to the classification of the product based
50.) Requirements for registration of local herbal on its therapeutic action as specified in the product
and/or traditional drugs: registration:
A. technical specifications of the ingredients A. pharmacologic category
used as component B. indication
B. Government certificate of clearance C. dosage form
C. free sale of drug D. dosage formulation
D. certification of the importation of the drug E. formulation
E. certification of the exportation of the drug
59.) It refers to the statement regarding the
51.) It is the science of philosophy of laws: occurrence of potential hazards and side effects
A. ethics associated with the use of the product
B. jurisprudence and the limitation of its use:
C. morality A. contraindication
D. rules B. warning
E. regulation C. precautions
D. indications
52.) It refers to viruses, sera, toxins and analogous E. pharmacologic category
products used for the prevention or cure of human
diseases: 60.) It refers to the instructions and special care
A. biologic products required in the use of product to avoid undesired
B. poison effects and to ensure the safe and effective use of the
C. device drug:
D. Both A and C A. contraindications
E. Both B and C B. warning
C. pharmacologic category
53.) An instrument, apparatus or contrivances, D. indications
including their components, parts, and accessories, E. precautions
intended for use in the diagnosis, cure, mitigation,
treatment or prevention of disease in man or other 61.) _____drugs not covered by patent protection and
animals: which are labeled solely by their international non-
A. device proprietary name:
B. drug A. generic
C. cosmetics B. innovator
D. poison C. branded
E. biologic products D. essential
E. non-essential
54.) Drug intended for use for animals:
A. poison 62.) The term “Drug Outlet” does not include:
B. antibiotics A. botica
C. new drugs B. drugstore
D. new veterinary drugs C. drug laboratory
E. biologic products D. Both A and B
E. none of the above
55.) Any drug intended for use by man containing any
quantity of any chemical substance which is produced 63.) It is an act providing protection to consumers by
by microorganism and which has the capacity to stabilizing the prices of basic necessities & prime
inhibit or destroy microorganism in dilute solution: commodities and by prescribing measures against
A. poison
undue price increases during emergency situations A. DDB
and like occasions: B. PDEA
A. RA 7394 C. FDA
B. RA 7581 D. DOH
C. RA 7432 E. PRC
D. RA 3720
E. RA 8293 71.) This refers to any facility used for the illegal
manufacture of any dangerous drug/or controlled
precursors and essential chemical:
64.) This order prescribes the conditions and A. classrooms
requirements for good manufacturing practice applied B. clandestine laboratory
to premises, equipment, personnel, product and C. licensed establishment
warehouse: D. all of the above
A. AO 220 E. none of the above
B. AO 42
C. AO56 72.) Maximum penalty shall be imposed if the sale,
D.AO 67 trading, administration, delivery or distribution of
E. AO 90 dangerous drugs and/or controlled precursor and
essential chemical transpires within ____meters from
65.) This order prescribes the activities involving drug school:
products that need to be covered by a licensed from A. 50
BFAD: B. 100
A. AO 220 C.101
B. AO 42 D.30
C. AO56 E. 10
D.AO 67
E. AO 90 73.) Penalty for unlawful prescription of dangerous
drugs:
66.) Under R.A 5921, administrative investigation A. fine of 100,000 pesos to 500,000 pesos
shall be conducted by all members of the Board of B. life imprisonment to death
Pharmacy. In case of suspension, it shall be for a C. fine of 500, 000 pesos to 10M pesos
period of NMT: D. b and c
A. 1 year E. a and c
B. 30 days
C. 6 months 74.) It refers to a licensed establishment carrying on
D. 60 days the retail business of sale of drugs and medicines to
E. 10 days customers:
A. exporter
67.) Under R.A 3720, if a drug’s strength differs from B. importer
or its safety, efficacy, quality or purity falls below the C. wholesaler
standards set forth in the compendium, then the drug D. retailer
is deemed to be: E. Both A and B
A. adulterated
B. mislabeled 75.) Penalty for illegal acts of price manipulation of
C. ineffective any drug and medicines subject to price regulation:
D. all of the above A. imprisonment of NLT 5 years nor more than
E. none of the above 15 years
B. fine of NLT 100,000 nor more than 10M
68.) Any person who shall be employed as detailman pesos
by any pharmaceutical establishment shall be C. imprisonment of NLT 10 years
required to register with the: D. imprisonment of NLT 5 YEARS
A. BFAD E. Both A and B
B. PRC
C. Board of Pharmacy 76.) _____contains the active ingredients and quantity
D. DOH of the drug per dosage unit:
E. PPhA A. dosage form
B. formulation
69.) If found guilty of neglect of duty, incompetence, C. mode of administration
malpractice, unprofessional or dishonorable conduct, D. excipient
after having been given the opportunity to defend E. preservatives
himself in administrative investigation, the Chairman
or members of the Board of Pharmacy may be 77.) Every prescription for external use filled in the
removed by: drugstore shall bear a red label showing in black ink
A. President of PACOP the components for such prescription and the word
B. President of the Philippines ______ at the bottom of the label:
C. PRC Commissioner A. “Warning: May be habit-forming”
D. Director of BFAD B. “For external use only”
E. President of PPhA C. “For internal use only”
D. “Flammable”
70.) A certified true copy of the record of dangerous E. “Inflammable”
drugs must be submitted to:
78.) The provision of this act on warranty shall not D. the number of counterfeit drug products is
applied to professional services of CPA, architects, NMT 3 brands
engineers, lawyers, veterinarians, optometrists, E. Both A and C
pharmacists, nurses, nutritionist, dieticians, physical
therapists, salesman, medical and dental practitioners 85.) Product which fails to comply with an applicable
and other professional engaged in their respective consumer product safety rule which creates a
professional endeavors: substantial risk of injury to the public is referred to:
A. RA 7581 A. misbranded
B.RA 7394 B. substandard
C. RA 7432 C. adulterated
D. RA 8293 D. expired
E. RA 8203 E. counterfeit

79.) ______for products other than biological products 86.) Basis for non-renewal of LTO:
means the date (month & year) during which the A. poor housekeeping
processing of the product, from which the goods are B. failure to comply with PRC standards and
to be filled is completed: requirements
A. expiry date C. serious, repeated or rampant violation of
B. date of distribution existing laws, rules & regulations
C. date of manufacture D. persistent performance that assures safety,
D. storage date efficacy and quality of drug products
E.stability E. All of the above

80.) Under A.O 55, the Rx symbol should be printed 87.) Only establishment with a valid LTO required
in a type size _____ of the height of the PDP: under _____ can apply to register a drug product:
A. NLT A. AO 56
B. NMT B. AO 62
C. NLT C. AO 55
D. NMT D.AO 90
E. None of the above E.AO 63

81.) The following persons shall be liable for 88.) Any person who is found guilty of “planting” any
violation(s) of RA 8203, except: dangerous drug and/or controlled precursor and
A. the manufacture of the counterfeit drugs essential chemical, regardless of the quantity and
B. importer or agents of counterfeit drugs purity shall suffer the penalty of:
C. the registered pharmacist who has actual A. Life imprisonment
or constructive knowledge about the B. death
counterfeit drugs C. Imprisonment from 6 years to 1 day to 12
D. the registered pharmacist who has no years
actual or constructive knowledge about the D. Imprisonment from 12 years to 20 years
counterfeit drugs E. Minimum penalty
E. exporter or agents of counterfeit drugs
89.) If the government officials and employees are
82.) If the unregistered imported drug product has a found guilty of the unlawful acts under RA 9165, they
registered counterpart brand in the Philippines, the shall be penalized by:
product shall be considered: A. perpetual absolute disqualification from any
A. acceptable for distribution public office
B. acceptable for importation B. imprisonment
C. Both A and B C. maximum penalty
D. counterfeit D. Both A and C
E. None of the above E. Both A and B

83.) ______shall mean, that by exercise of 90.) An establishment where pharmaceuticals,

reasonable care, one would have known the fact or proprietary medicines or pharmaceutical specialties
suspect that the drug product he or she has sold or in are prepared, compounded, standardized, and
possession of is counterfeit, such as but not limited to distributed or sold:
the knowledge, that the drug was not covered by any A. botica
sales invoice or evidence of delivery or purchase from B. Pharmaceutical Laboratory
a BFAD licensed establishment: C. Pharmaceutical Manufacturing Laboratory
A. constructive knowledge D. Both B and C
B. destructive knowledge E. Both A and B
C. limited knowledge
D. suspicious 91.) It is any drug, active principle or preparation of
E. full knowledge the same, capable of destroying life or seriously
endangering health when applied externally to the
84.) The maximum administrative penalty shall be body or introduced internally in moderate doses:
imposed when the counterfeit drug products are: A. biologic products
A. not life-saving drug products B. poison
B. life-saving regardless of the volume C. abortive products
C. the volume of the product is more than D. all of the above
100,000 pesos E. none of the above
 99.) It is composed of a core list of medicines
92.) An articles intended for use in the diagnosis, considered essential and a complementary list of
cure, mitigation, treatment or prevention of disease in drugs considered useful if not essential:
man and animals: A. National Drug Policy (NDP)
A. device B. National Drug Formulary (NDF)
B. drugs C. National Drug Committee (NDC)
C. cosmetics D. none of the above
D. poison E. all of the above
E. none of the above 100.) It is a team of pharmacologist, pharmacists and
clinicians whose main task is to prepare the National
93.) The date stated in the label of a drug or device Drug Formulary and recommend to the BFAD the
after which the drug is not expected to retain its drug for delisting:
claimed safety, efficacy, and quality or potency or A. National Drug Policy (NDP)
after which it is not permissible to sell the drug or B. National Drug Formulary (NDF)
device: C. National Drug Committee (NDC)
A. manufacturing date D. none of the above
B. registration date E. all of the above
C. production date
D. stability date 101.) It is the description of the chemical structure of
E. expiration date the drug or medicine and serves as the complete
identification of a compound:
94.) It is the pharmaceutical form of the preparation A. chemical name
based on official pharmacopeia: B. generic name
A. pharmacologic category C. INN
B. indication D. Both B and C
C. dosage formulation E. Both A and C
D. dosage form
E. dosage 102.) It is the finished product form that contains the
active ingredients, generally but not necessarily in
95.) The process of approval for the manufacture, association with inactive ingredients:
importation, exportation, sale, offer for sale, A. drug product
distribution or transfer of pharmaceutical products B. generic drug
containing active ingredient/s of known chemical C. essential drug
structure and properties determined to be safe, D. drug innovator
efficacious, and of good quality according to E. Investigational drug
standards of BFAD:
A. CGMP 103.) It is the act by a validly registered pharmacist of
B. registration filling a prescription or doctor’s order on the patient
C. assay chart:
D. drug evaluation A. delivering
E. licensing B. selling
C. dispensing
96.) It is a drug, the safety and efficacy of which has D. trading
been demonstrated through long years of general use E. counseling
and can be found in the current official USP-NF, and
other internationally recognized pharmacopeias: 104.) It refers to the branch of medical science
A. investigational drugs devoted to the study of the biological and physical
B. established drugs changes and the disease of old age:
C. new drugs A. pediatrics
D. tried and tested drugs B. pharmacy
E. Innovative drugs C. geriatrics
D. orthodontics
97.) It is a policy and program of the national E. obstetrics
government to ensure that safe and effective drugs
are made available to all Filipinos at any time and 105.) These drugs may be dispensed even without a
place and at a reasonable and affordable cost: written order of a validly registered physician, dentist
A. National Drug Policy (NDP) or veterinarian in duly licensed drug outlets:
B. National Drug Formulary (NDF) A. ethical drugs
C. National Drug Committee (NDC) B. OTC drugs
D. none of the above C. prescription drugs
E. all of the above D. dangerous drugs
E. vitamins
98.) It is a special group within the DOH which
oversees the implementation of the NDP: 106.) It means a natural person who is a purchaser,
A. NDP Management Committee lessee, recipient or prospective purchaser, leaser or
B. National Drug Formulary (NDF) recipient of consumer products, services or credits:
C. National Drug Committee (NDC) A. creditor
D. none of the above B. consumer
E. all of the above C. customers
D. owner
E.lessor
 commodities grossly in excess of their normal
107.) It means any substance which on contact with requirements resulting in undue shortages of such
living tissue will cause destruction of tissue by goods to the prejudice of less privileged consumers:
chemical action: A. hoarding
A. corrosive B. panic buying
B. poison C. cartel
C. antibiotics D. profiteering
D. biological E. bargain
E. antiseptic
115.) It is a contingent fund in the budget of the
108.) It means any device, written, printed, affixed or implementing agency which shall not be used in
attached to a consumer product or displayed in a normal or regular operations but only for the purposes
consumer repair or service establishment for the provided under the Price Act:
purpose of indicating the retail price per unit or A. petty cash
service: B. buffer fund
A. label C. Both A and B
B. price tag D. NOTA
C. sticker E. allocation fund
D. ID tag
E. lanyard 116.) It is the maximum price at which an basic
necessities or prime commodities may be sold to the
109.) Any person engaged in the business of selling general public:
consumer products directly to consumers: A. prevailing price
A. supplier B. price ceiling
B. exporter C. discounted price
C. telemarketing D. 50% off of the original price
D. retailer E. 25% off of the original price
E. importer
117.) The illegal cultivation, culture, delivery,
110.) It is the undue accumulation by a person or administration, dispensation, manufacture, scale,
combination of persons of any basic necessity or trading, transportation, distribution, importation,
prime commodity beyond his or their normal inventory exportation and possession of any dangerous drugs
levels: and/or controlled precursor and essential chemicals:
A. hoarding A. illegal trafficking
B. panic buying B. illegal cultivation
C. cartel C. illegal selling
D. profiteering D. illegal possession
E. hoarder E. illegal compounding

111.) An analytical test using a device, tool or 118.) Shabu:

equipment with a different chemical or physical A. Methylenedioxymethamphetamine
principle that is more specific which will validate and B. Methyldioxymethamphetamine
confirm the result of the screening test: C. MMDA
A. confirmatory test D. Methamphetamine Hydrochloride
B. screening test E. Methamphetamine
C. drug analysis
D. NOTA 119.) Ecstacy:
E. All of the above A. Methylenedioxymethamphetamine
B. Methyldioxymethamphetamine
112.) It is any combination of or agreement between C. MMDA
two or more persons engaged in the production, D. Methamphetamine Hydrochloride
manufacture, processing, storage, supply, distribution, E. Methamphetamine
marketing, sale or disposition of any basic necessity
or prime commodity designed to artificially and 120.) A rapid test performed to establish
unreasonably increased or manipulate its price: potential/presumptive positive result:
A. hoarding A. confirmatory test
B. panic buying B. screening test
C. cartel C. test analysis
D. profiteering D. laboratory test
E. bargain E. Physico-chemical test

113.) The sale or offering for sale of any basic 121).Indian hemp
necessity or prime commodity at a price grossly in A. marijuana
excess of its true worth: B. hashish
A. hoarding C. bhang
B. panic buying D. all of the above
C. cartel E. NOTA
D. profiteering
E. bargain 122. It refers to the international agreement
114.) It is the abnormal phenomenon where administered by the WTO that sets down minimum
consumers buy basic necessities and prime standards for many forms of intellectual property
regulations: Intellectual Property Rights
A. TRIPS Agreement D. both a and c
B. WTO Agreement E. both a and b
C. Agreement on Trade- Related Aspects of

123. Amendments to A.O 62: D. “shake well”

A. A.O 90, s. 2002 E. reconstitute
B. A.O 90, s. 1990
C. A.O 42 132. The potency of biological products must be
D. A.O 56 expressed in
E. A.O 64
A. metric system
124. Requirements for Labelling Materials of B. apothecary
Pharmaceutical Products C. international unit
A. A.O 55 D. avoirdupois
B. A.O 90 E. SI system
C. A.O 42
D. A.O 56 133. These are drugs found in the USP/NF and is
E. A.O 63 considered safe and efficient through long years of
general use
125. The Price Act is known as R.A A. Investigational
A. 7432 B. Established
B. 7581 C. New
C. 8293 D. Tried & Tested
D. 7394 E. Essential
E. 7349
134. Basis for non- renewal of LTO of Drug Outlet &
126. Number of years of pharmacy practice for the Drug Establishment
pharmacist to qualify as board examiner A. failure to comply with PRC standards and
A. 5 years requirements
B. 10 years B. serious repeated or rampant violation of existing
C. 15 years laws, rules & regulations
D. 20 years C. persistent performance that assures the safety,
E. 2 years efficacy & quality of drug products
D. poor housekeeping
127. R.A 9165 was signed into law on E. Minor shortcomings
A. June 7, 2002
B. February 26, 2004 135. Drug classification based on source
C. June 23, 1969 A. branded & patented
D. June 22, 1963 B. imported as finished
E. July 7, 2002 C. unbranded & off patient
D. both a and c
128. Upon finding that the drugs are counterfeit, the E. both a and b
Bureau shall file an appropriate proceeding against
the registered pharmacist with the PRC for the 136. The BFAD must be notified of such charge in the
of professional license______ establishment
A. suspension A. change of manager
B. cancellation B. change of pharmacist-in-charge
C. revocation C. change of product arrangement
D. both a and c D. change of supervisor
E. both a and b E. change of pharmacist- assistant

129. The Board of Pharmacy is composed of a 137. The BOP, upon receipt of a formal complaint
Chairman and___________members under oath against any pharmacist, shall furnish the
A. 4 latter a copy of the complaint which he shall answer
B. 3 within
C. 2 A. 30 days
D. 5 B. 10 days
E. 6 C. 60 days
D. 6 months from receipt
130. The net content of the liquid dosage form must E. 15 days
be expressed using
A. Arabic numeral & avoirdupois system 138. Any product that is not labelled in accordance
B. metric system with the requirements of A.O 55 shall be deemed
C. Arabic numeral & metric system A. misbranded
D. Roman numeral & avoirdupois system B. conforms with the USP/NF standards
E. Roman numeral C. both a and b
D. NOTA
131. It indicates that the product is a prescription drug E. Adulterated
A. Rx symbol
B. for external use 139. The sale of physician’s sample is a prohibited act
C. a vignette of skull & bones under R.A
A. 3720
B. 9275 B. PNP Chief
C. 6675 C. Secretary of Health
D. 9502 D. Director General
E. 5921 E. Director

140. Misrepresentation of any material fact in the 148. Prescription for dangerous drugs are written in
application of LTO for a drug establishment is a A. duplicate
ground for B. triplicate
C. one copy
A. cancellation of the professional license of the said D. any of the above
pharmacist E. One original and one duplicate
B. suspension of the LTO
C. revocation of the LTO 149. The following are exempted from complying with
D. temporary closure the labelling requirements, except
E. permanent closure A. if the products are used solely for investigational
use B. if the
141. Failure to properly record dangerous drugs as products are compounded by the pharmacist
determined by the DDB in a drug outlet is a ground for C. established drugs
A. cancellation of the professional license of the said D. if the products are donated by foreign agencies
pharmacist E. All of the above
B. suspension of the LTO
C. revocation of the LTO 150. Any herbal and/ or traditional drug the
D. temporary closure registration of which is not intended to be renewed
E. permanent closure may be given an extension of NMT
A. 30 days
142. Absence of pharmacist in a drugstore on three B. 10 days
inspections by BFAD inspector is a ground for C. 60 days
A. cancellation of the professional license of the said D. 6 months after the expiry date of such registration
pharmacist E. 3 months after the expiry date of such registration
B. suspension of the LTO
C. revocation of the LTO 151. It is the science of morality
D. temporary closure A. ethics
E. permanent closure B. jurisprudence
C. morality
143. Non- pharmacist may owned and open a D. rules
drugstore provided that there is a E. both a and c
A. supervisor
B. pharmacist assistant 152. It is identified by the willingness of individual
C. pharmacy technician practitioners to comply with ethical and professional
D. registered pharmacist standards which exceed minimum legal requirements
E. manager A. jurisprudence
B. ethics
144. Violations of any provision of Senior Citizens Act C. both a and b
is punishable by D. profess
A. a fine not exceeding 2, 000 pesos E. profession
B. imprisonment of NLT 2 months but NMT 2 years
for the first offense 153. It pertains to the ability to engage in sound moral
C. imprisonment not exceeding 2 months reasoning and consider carefully the implications of
D. a fine of 5, 000 pesos but not exceeding 10, 000 alternative actions
pesos A. ethical awareness
E. imprisonment of NLT 6 months but NMT 2 years B. laws
for the first offense C. ethical competency
D. jurisprudence
145. The discount privileges of the senior citizens E. ethics
shall be
A. transferable but limited to use only for the senior 154. It means a system of words or other systems
citizen arbitrarily used to represent words
B. non- transferable A. code
C. limited and exclusive for the benefit of the senior B. secret keys
citizen C. secret clues
D. both b and c D. cipher
E. NOTA E. coding

146. Registration of herbal and/or traditional drugs 155. An articles used for food or drink of man
must be renewed every A. device
A. year B. drug
B. 2 years C. food
C. 3 years D. poison
D. 5 years E. herbal drugs
E. 6 years
156. A quantity of any drug or device produced during
147. Head of the PDEA a given cycle of manufacture
A. NBI Chief A. batch
B. lot A. volume
C. batch number B. strength
D. lot number C. Total net
E. group D. potency
E. net content
157. Any ingredient intended for use in the
manufacture of a product, which include raw and 165. It refers to the part of the label that is most likely
packaging materials, including those that may not to be displayed, presented, shown or examined under
appear in the finished product customary conditions of display for retail use
A. component A. Principal Display Panel
B. raw material B. Primary Pack
C. both a and b C. Area of the Principal Display Panel
D. none of the above D. inserts
E. all of the above E. Package inserts

158. Any substance including food additive, used as a 166. The first pack containing the individually
component in the manufacture or preparation of a wrapped products, strips, or blister packs
food and present in the final product in its original or A. wrapper cartons
modified form B. inserts
A. raw material C. primary pack
B. minute organism D. leaflets
C. microorganism E. Area of the Principal Display Panel
D. inactive
E. ingredient 167. Any establishment which is a registered owner of
the drug product, procures the raw materials and
159. It refers to the proprietary name assigned to the packaging components, and provides the production
product by the drug establishment monographs, quality control standards and
A. trade name procedures, but sub- contracts the manufacture of
B. brand name such product to a licensed manufacturer
C. both a and b A. Drug Manufacturer
D. generic name B. Drug Trader
E. INN C. Drug Importer
D. Drug Exporter
160. It refers to the identification of drugs and E. Drug Distributor
medicine by their scientifically and internationally
recognized active ingredient as determined by the 168. A drug approved for sale to the general public
BFAD of the Department of Health under certain conditions
A. trade name A. Drug for Restricted Use
B. brand name B. Drug for General Use
C. both a and b C. Drug for Limited Use
D. generic name D. Drug for registration
E. proprietary name E. None of the above

161. Refers to the name/s and amount/s of active 169. It is a certification issued after a batch of
medicinal ingredients per dosage unit expressed in antibiotics has been found to comply with the
the metric system characteristics to identity, strength, quality and purity
A. net content A. certificate of Good Standing
B. formulation B. Batch Certification
C. strength C. Certificate of Product Registration (CPR)
D. potency D. CGMP
E. Total amount E. GMP

162. It refers to the site and manner the product is to 170. It refers to the standards and procedures
be introduced into or applied in the body whereby the laboratory achieves a defined, consistent
A. device and reliable standard in performing laboratory tests
B. directions of use and activities
C. method of determination A. GMP
D. route of administration B. GCP
E. mode of administration C. GLP
D. CPR
163. It refers to the statements regarding the E. GCP
conditions wherein the use of the product may cause
harm to the patient 171. It is a document issued by the BFAD for the
A. contraindications purpose of marketing, use of free distribution of a
B. warning product in the Philippines
C. precautions A. Certificate of Good Standing
D. indications B. Batch Certification
E. Pharmacological use C. CGMP
D. Certificate of Product Registration (CPR)
164. It refers to the total amount/quantity/number of E. GCP
the dosage form in a certain container of a product
expressed in metric system
172. It refers to the standards and procedures for A. standard
clinical trials that encompasses the design, protocol, B. services
conduct, monitoring, termination, audit, analyses, C. labor
reporting, and documentation of human studies D. all of the above
A. GMP E. none of the above
B. GCP
C. GLP 181. It includes rice, corn, bread, fish and drugs
D. CPR classified as essential by the Department of Health
E. Batch Certification A. Basic necessities
B. prime commodities
173. It means the label on or affixed to an immediate C. primary needs
container D. all of the above
A. outer label E. none of the above
B. inner label
C. immediate label 182. Any act of knowingly planting, growing, raising,
D. principal display panel or permitting the planning of any plant which is the
E. primary pack source of dangerous drugs
A. cultivate
174. It means a display of written, printed or graphic B. culture
matter upon any article or any of its containers or C. pusher
wrappers or attached to or accompanying such D. both b and c
articles E. both a and b
A. principal display panel
B. leaflets 183. Any act of knowingly passing a dangerous drug
C. label to another, personally or otherwise, and by means,
D. package material with or without consideration
E. primary pack A. cultivate
B. deliver
175. It refers to a drug products indicated for life C. culture
threatening conditions D. both a and c
A. lifesaving drugs E. both a and b
B. counterfeit drugs
C. drugs for limited use 184. Any person who is a licensed physician, dentist,
D. drugs for restricted use chemist, medical technologist, nurse, midwife,
E. Dangerous drugs veterinarian or pharmacist in the Philippines
A. practitioner
176. It is a list of drugs that meet the health care B. coddler
needs of the majority of the population C. protector
A. EDL D. pusher
B. complementary list E. professional
C. NDF
D. Generic drugs list 185. It refers to drugstores, pharmacies, and other
E. core list business establishments which sell drugs and
medicines
177. It is a written order and instruction of a validly A. Drug Outlet
registered physician, dentist or veterinarian for the B. Drug Establishment
use of a specific drug product for a specific patient C. Drug Laboratory
A. prescription D. both b and c
B. medical chart E. All of the above
C. purchase slip booklet
D. Medical order 186. Any change in the law can be done by passing
E. none of the above a/an
A. memorandum order
178. Based on RA 9527, any resident citizen of the B. amendments
Philippines at least sixty (60) years old C. bill
A. senior citizen D. administrative order
B. neonates E. Executive order
C. elderly
D. pediatrics 187. The minimum age requirement to practice
E. both a and c pharmacy in the Philippines
A. 18
179. It means any card, plate, coupon book, or other B. 19
credit device existing for the purpose of obtaining C. 20
money, property labor or services on credit D. 21
A. credit card E. 22
B. ATM card
C. ID card 188. The book kept for the purpose recording the sale
D. value card of violent poisons should be preserved for a period of
E. Discount card A. 1 year
B. 2 years
180. It means a set of conditions to be fulfilled to C. 4 years
ensure quality and safety of a product
D. 5 years 198. Amount of shabu subject to life imprisonment to
E. 3 years death and a fine ranging from 500, 000 pesos to 10M
pesos
189. Ordinary prescriptions shall be retained by the A. 500g
pharmacist for a period of B. 10g
A. 1 year C. 50g
B. 2 years D. 40 g
C. 4 years E. 20g
D. 5 years
E. 3 years 199. Amount of opium subject to life imprisonment to
death and a fine ranging from 500, 000 pesos to 10M
190. The Rx symbol is required in the label of pesos
A. ethical drugs A. 500g
B. Over-the-Counter drugs B. 10g
C. prescription drugs C. 50g
D. both a and c D. 40 g
E. both a and b E. 20g
191. Amendments of A.O 55 200. Duration of the conduct of examination in
A. A.O 67 determining the genuineness and authenticity of the
B. A.O 90 product Bureau
C. A.O 64 A. 10 working days
D. A.O 56 B. 20 working days
E. A.O 63 C. 16 working days
D. within 24 hours
192. The Foods, Drugs, Devices and Cosmetics Act is E. within 36 hours
known as R.A
A. 5921 201. The senior citizens shall be entitled the grant of
B. 6675 discount for the consumption of electricity, water and
C. 3720 telephone by the senior citizens center and residential
D. 8203 care/group homes that are non- stock, non- profit
E. 3702 domestic corporation
A. 20%
193. The Pharmacy Law is known as R.A B. 50%
A. 5921 C. 10%
B. 6675 D. 5%
C. 3720 E. 25%
D. 8203
E. 3702 202. The senior citizens shall be entitled the grant of
discount from all establishments relative to the
194. The Consumers Act of the Philippines is known utilization of transportation services, restaurants and
as R.A purchase of medicines anywhere in the country,
A. 7432 including funeral & burial services for the death of the
B. 7581 senior citizens
C. 8293 A. 20%
D. 7394 B. 50%
E. 8203 C. 10%
D. 5%
195. The Expanded Senior Citizens Act of 2003 is
E. 25%
known as R.A
A. 9257 203. For Drug Establishment, re- application of the
B. 7581 LTO after revocation may be done within
C. 8293 year/s________
D. 7394 A. 2
E. 7432 B. 3
C. 1
196. Filling and refilling of prescription shall be done
D. 5
by
E. 4
A. intern with the supervision of the registered
pharmacist 204. R.A 5921 was signed into law on
B. RPh A. June 7 2002
C. pharmacist assistant B. February 26, 2004
D. supervisor C. June 23, 1969
E. clinicians D. June 22, 1963
E. June 23, 1963
197. A certain drug is considered counterfeit if it
contains less than how many percent of the active 205. This is the division of the BFAD that provides
ingredient it purports to possess assistance to person/establishment in complying with
A. 10 BFAD legal requirements
B. 40 A. Product Services
C. 80 B. Laboratory Services
D. 95 C. Legal, Information and Compliance
E. 20
D. Administrative 215. Under R.A 6675, which of these prescriptions
E. Regulation Division I shall be filled
A. violative Rx
206. The division of BFAD that certifies batches of B. erroneous Rx
antibiotics C. impossible Rx
A. Product Services D. both a and c
B. Laboratory Services E. none of the above
C. Legal, Information and Compliance
D. Administrative 216. Has the power to reclassify, add to, or remove
E. Regulation Division I any drug from the list of dangerous drugs
A. DDB
207. The division of BFAD that is involves in cash B. PDEA
collection C. BFAD
A. Product Services D. NBI
B. Laboratory Services E. DOH
C. Legal, Information and Compliance
D. Administrative 217. The BFAD shall be headed by a
E. Regulation Division I A. President
B. Secretary
208. The permanent consultant/s of the Dangerous C. Director
Drug Board D. Commissioner
A. PNP Chief E. Chief
B. NBI Director
C. both a and b 218. Any person desiring to operate or establish a
D. Secretary of Health drug establishments shall file with the BFAD an
E. both b and d application supported by the following documents,
except
209. Executive Order which is responsible in A. red & white labels indicating the name of the
reorganization of BFAD drugstore
A. 175 B. proof of registration
B. 851 C. list of products to be manufactured identified by its
C. 119 generic and brand names
D. 174 D. current PTR of the pharmacist-in-charge
E. 803 E. both a and b
210. Additional label to be attached to the poisons 219. Unless otherwise declared by the President,
A. warning: may be habit- forming prices of the basic necessities in an area shall
B. warning it is toxic automatically be frozen at their prevailing prices or
C. a vignette of skull & bones placed under automatic price control whenever that
D. for internal use area is
E. all of the above A. declared to be in state of rebellion
B. is placed under martial law
211. The designated person of a manufacturing C. is under state of calamity
company who will transact officially with the Bureau D. all of the above
A. branch pharmacist E. only b and c
B. liaison officer
C. detail man 220. Based on R.A 9165, sec. 15, the penalty
D. supervisor imposed upon any person apprehended or arrested
E. branch manager for the first time, who is found to be positive for use of
any dangerous drug, after a confirmatory test is
212. In the labelling requirements, the generic name A. a minimum of 6 months rehabilitation in a
must be government center
A. enclosed by an outline circle B. imprisonment ranging from 6 yrs and one day to
B. smaller font size than the brand name twelve years
C. written after the brand name C. a fine of 50, 000 pesos to 200, 000 pesos
D. printed in full and not abbreviated D. both a and b
E. Different font with the brand name E. both b and c
213. The word “single use” must be included in the 221. Based on R.A 9165, sec. 15, the penalty
label of imposed upon any person apprehended or arrested
A. biological products for the second time, who is found to be positive for
B. small containers use of any dangerous drug, after a confirmatory test is
C. individually wrapped products A. a minimum of 6 months rehabilitation in a
D. large volume injection government center
E. small volume injection B. imprisonment ranging from 6 yrs and one day to
twelve years
214. A drug product prescribed which is not registered
C. a fine of 50, 000 pesos to 200, 000 pesos
at BFAD is considered a type
D. both a and b
A. impossible Rx
E. both b and c
B. violative Rx
C. erroneous Rx 222. Serves as the implementing arm of the DDB
D. coded Rx A. BFAD
E. Rx
B. DOH B. R.A 9257
C. NBI C. R.A 9502
D. PDEA D. R.A 8485
E. PNP E. R.A 9994

223. A food shall be deemed to be misbranded if 231. An act to promote, require, and ensure the
A. it consists in whole or in part of any filthy or putrid production of an adequate supply, distribution, use,
substances and acceptance of drugs and medicines identified by
B. its labelling is false or misleading their generic names
C. it contains any poisonous or deleterious A. R.A 3720
substances B. R.A 6675
D. both a and c C. R.A 9165
E. both a and b D. R.A 9502
E. R.A 9257
224. A food shall be deemed to be adulterated if
232. An act instituting the Comprehensive Dangerous
A. it consists in whole or in part of any filthy or putrid Drugs Act of 2002, repealing R.A 6425, as amended,
substances providing funds therefore, and for other purposes
B. its labelling is false or misleading A. R.A 3720
C. it contains any poisonous or deleterious B. R.A 6675
substances C. R.A 9165
D. both a and c D. R.A 6425
E. both a and b E. R.A 9502
225. The members of the Board of Pharmacy are 233. An act to ensure the safety & purity of foods &
appointed by the cosmetics, and the purity, safety, efficacy and quality
A. PRC commissioner of drugs and devices being made available for the
B. PACOP President public, vesting the BFAD with authority to administer
C. PPhA President &enforce the laws pertaining thereto, & for other
D. President of thePhilippines purposes
E. CHED Commissioner A. R.A 3720
B. R.A 6675
226. To recognize and accredit colleges and schools C. R.A 9165
of pharmacy in the different colleges and universities D. R.A 6425
is a function of a E. R.A 9502
A. Board of Pharmacy
B. PRC 234. This Act shall be known as the “Food and Drug
C. Council of Pharmaceutical Education Administration (FDA) Act of 2009
D. PPhA A. R.A 9994
E. PACUCOA B. R.A 9165
C. R.A 9165
227. To reprimand any erring pharmacist or to D. R.A 9257
suspend or revoke his certificate of registration is a E. R.A 9711
function of
A. Board of Pharmacy 235. A candidate for Pharmacy board examination in
B. PRC the Philippines shall have the following qualification/s
C. Council of Pharmaceutical Education A. natural- born Filipino citizen
D. PPhA B. graduated with any four year course
E. FDA C. of good moral character
D. all of the above
228. The minimum mandatory requirements E. none of the above
necessary for the opening and operation of
drugstores and pharmacies shall be in a accordance 236. What type of font was specified for printing the
with the rules and regulations prescribed by the generic name if the name of the product is presented
A. BFAD using a special typeface exclusively designed for it
B. DOH A. comic sans
C. DDB B. Helvetica Medium
D. PDEA C. Universe Medium
E. PRC D. both b and c
E. both a and c
229. An act regulating the practice of pharmacy &
setting standards of pharmaceutical education in the 237. In accordance to A.O 56, s. 1989, the initial LTO
Philippines and for other purposes has a validity of_______ years
A. R.A 3720 A. 5
B. R.A 5921 B. 3
C. R.A 9165 C. 2
D. R.A 9502 D. 1
E. R.A 9994 E. 4
230. An act providing for cheaper & quality medicines 238. Under A.O 56, s. 1989, the renewal of the LTO
amending for the purpose R.A 8293, R.A 6675 and has a validity of ________years
R.A 5921, and for other purposes A. 5
A. R.A 9165
B. 3 C. products placed in small containers
C. 2 D. drugs for investigational purposes
D. 1 E. small volume injection
E. 4
248. Pharmacy Licensure Examination in the
239. Under R.A 9165, the penalty of 12 years and one Philippines is held
day to 20 years of imprisonment and a fine of 100, A. once a year
000 pesos to 500, 000 pesos shall be imposed upon B. twice a year
any person who acts as a C. every other year
A. coddler D. every December
B. financier E. thrice a year
C. protector
D. compounder 249. Refusal to allow entry of BFAD inspector is
E. either a and c penalized by
A. suspension of LTO
240. Production records must be kept for B. revocation of LTO
A. 2 years before expiration date C. temporary closure
B. 2 years after batch distribution is completed D. cancellation of LTO
C. 2 years after expiration date of the product E. permanent closure
D. 1 year after batch distribution is completed
E. 1 year after batch distribution is completed 250. It is composed of a core list of medicines
considered essential and a complimentary list of
241. This is the required test for suppositories and drugs considered useful if not essential
pessaries A. MMS
A. weight variation B. PDR
B. boiling point C. Goodman & Gillman
C. melting point D. National Drug Formulary (NDF)
D. dissolution E. EDL
E. hardness
251. Monitors the treatment and rehabilitation of drug
242. Which Executive Order abolished the Food and dependents and operation of drug rehabilitation and
Drug Administration and created the BFAD testing centers
A. EO174 A. PDEA
B. EO 851 B. BFAD
C. EO 175 C. NBI
D. EO 815 D. DOH
E. EO 119 E. PNP

243. The government agency which issues national 252. It means to bring into the Philippines by sea,
ID card and purchase slip booklet land or air
A. BFAD A. import
B. DOH B. distribute
C. OSCA C. export
D. PHILHEALTH D. manufacture
E. none of the above E. shipping

244. This means dispensing the patient’s or buyer’s 253. It means the delivery or sale of any drug or
choice from among the generic equivalent device for purposes of distribution in commerce,
A. generic dispensing except that such term does not include a
B. dispensing manufacturer or retailer of such product
C. any of the above A. import
D. NOTA B. distribute
E. all of the above C. export
D. manufacture
245. The former President of the Philippines who E. both a and c
enunciated the National Drug Policy
A. Ferdinand E. Marcos 254. Quality control requirements for herbal and/or
B. Joseph Estrada traditional drugs
C. Corazon C. Aquino A. test for the presence of heavy metals
D. Ramon Magsaysay B. test for the presence of synthetic drugs
E. DiosdadoMacapagal C. test for alcohol content
D. all of the above
246. CGMP means E. none of the above
A. current good manufacturing practice
B. current good manufacture process 255. Pursuant to A.O 55, all information required to
C. current good manufacture process appear on the label must be
D. current good manufacturing procedure A. written in English
E. none of the above B. clearly and prominently displayed
C. readable with normal vision with straining
247. Which of the following is exempted in the D. all of the above
labelling requirement E. none of the above
A. large volume injection
B. product for external use
256. INN means 264. The expiry date of the product shall be
A. International Non- proprietary name expressed I terms of the:
B. International Propriety Name A, month and year
C. Intentional Non- Proprietary Name B. month, date and year
C. year
D. International Name D. date and year
E. International Property Name E. none of the above

257. Based on the PNDF, the following are drugs 265. Requirements for registration of “Me- Too” or
acting on then CNS, except: identical products include:
A. anti-gout A. toxicology data
B. anti-schistosoma B. pharmaceutical from of the drug
C. anti-parkinsonism C. clinical investigation data
D. anti-vertigo D. mutagenicity
E. anti- lipidemic E. LD 50

258. Based on the PNDF, the following are Gastro- 266. It is the consistency system of quality assurance
Intestinal drugs, except: aimed at ensuring that products are consistently
A. anti- lipidemic manufactured to a quality appropriate for intended
B. anticholinergic use:
C. spasmolytic A. GLP
D. antacid B. GCP
E. anti-gout C. CGMP
D. CPL
259. The division in BFAD that evaluates and E. CPR
processes application for the registration of all
products under BFAD’s jurisdiction: 267. All prescriptions dispensed in the drugstore,
A. LSD botica or hospital pharmacy shall; be kept on file for:
B. PSD A. one year
C. LICD B. 2 years
D. Regulation Division II C. 3 years
E. Administrative Division D. 4 years
E. 5 years
260: The division in BFAD that conduct all test
analyses and trials of products under BFAD’s 268. Partial filling of prescription for drugs belonging
jurisdiction: to List A shall:
A. LSD A. be allowed
B. PSD B. not be allowed
C. LICD C. is allowed provided that the S-2 of the prescriber is
D. Regulation Division II indicated.
E. Administrative Division D. be allowed provided that a yellow prescription was
presented
261. The division in BFAD that conducts E. both c and d
administrative or quasi-judicial hearings and
recommends imposes appropriate legal action: 269. An acting granting additional benefits and
A. LSD privilege to senior citizens amending of the purpose
B. PSD RA 7432:
C. LICD A. R.A. 9165
D. Regulation Division II B. R.A. 9257
E. Administrative Division C. R.A. 9502
D. R.A. 8485
262. The division in BFAD that calls upon any erring E. R.A. 9711
manufacturer, distributor or advertiser to desist from
inaccurate or misleading nutritional or medical claims 270. OTC- that requires batch certification:
in their advertising: A. OTC drugs
A. LSD B. dangerous drugs
B. PSD C. prescription drugs
C. LICD D. antibiotics
D. Regulation Division II E. biological
E. Administrative Division
271. Minimum penalty shall be imposed if the
263. It refers to the prevailing specified range of counterfeit drug product is:
temperature, humidity, and other environmental A. life-saving
factors within optimal stability of the product: B. not life-saving
A. storage conditions C. both a and b
B. temperature range D. dangerous drugs
C. stability E. none of the given choice
D. expiry date
E. Humidity range 272. Government office where professional register
and where license is issued:
A. PRC
B. BFAD C. 4
C. BFAD D. 5
D. DDB E. 1
E. DOH
281. In order to manufacture, sell, offer for sale,
273. Acts as the policy formulation and sectors import or distribute any drug or device, a license to
monitoring arm of the Secretary of Health on matters operate should be first secured from:
pertaining to foods, drugs, traditional medicines, A. BFAD
cosmetics and household products containing B. DTI
hazardous substances: C. PRC
A. Director of PDEA D. PRC
B. DDB Director E. BOP
C. BFAD Director
D. President of PPhA 282. The term “elderly “shall means
E. None of the above A. senior citizen
B. any resident of the Philippines
274. Collects samples of products in outlets under C. at least 60 years old
BFAD jurisdiction for laboratory analysis: D. all of the above
A. Regulation division I E. none of the above
B. Regulation division II
C. LSD 283. The term Secretary, in RA 3720, means:
D. PSD A. Secretary of DOH
E. LICD B. Secretary of DTI
C. Secretary of Education
275. Assist in the development of the short/long range D. all of the above
plan and prepares the budget estimates of BFAD: E. none of the above
A. Office of the director
B. LICD 284. Prescription for dangerous drugs are written in:
C. PSD A. triplicate
D. Regulation Division II B. duplicate
E. Administrative Division C. five
D. Four copies
276. Coordinates the activities of the Drug Information E. One copy
Unit (DIU) for the purpose of information
dissemination 285. It refers to any establishment that imports raw
A. Office of the Director materials active ingredients and finished products for
B. Administrative Division its own use or for distribution to other drug
C. LICD establishments or outlets:
D. Regulation Division I A. exporter
E. Regulation Division II B. importer
C .wholesaler
277. Laboratory controls are required for: D. retailer
A. finished product E. none of the above
B. components
C. in process drug 286. Under RA 3720, Food means:
D. all of the above A. chewing gum
E. none of the above B. articles used for food or drink for man
C. a and b
278. Ointments, creams, and other semi-solid D. NOTA
preparations are tested for: E. nutraceuticals
A. melting point
B. homogeneity 287. Who shall take care and deliver to the Bureau
C. impalpability the samples taken at random from every incoming
D. all of the above shipment of food, drugs, devices and cosmetics which
E. none of the above are being imported or offered for import into the
Philippines?
279. As defined in RA 8203, this refers to any entity, A. Secretary of Health
whether a single proprietorship, partnership or B. BFAD Director
corporation engaged in or doing business in the C. Commissioner of Customs
Philippines: D. a and b
A. residency E. b and c
B. business establishment
C. brokering 288. Based on RA 3720, any poisonous or deleterious
D. ownership substance added to any food shall be deemed to be
E. franchising unsafe except when such substance is required or
cannot be avoided in its production of manufacture:
280. for how many years shall the chairman and A. the statement is incorrect
members of the Board of Pharmacy hold office after B. the statement is correct
appointment: C. only deleterious substance added
A. 2 D. all of the above
B. 3 E. NOTA
 C. February 7, 1992
289. Minor deficiencies in GMP includes, except: D. September 13, 1988
A. inadequate storage facilities E. June 22, 1963
B. lack of minor equipment
C. lack of key technical and professional personnel 296. R.A. 7432 was signed into law on:
D. poor housekeeping A. April 13, 1992
E. inadequate storage facilities B. February 26, 1992
C. February 7, 1992
290. Drugs are considered to be adulterated if: D. September 13, 1988
A. it differs from USP standards E. June 22, 1963
B. it is an imitation of another product
C. the label is misleading 297. It is an analysis to determine the presence of a
D. both a and c substance and the amount of that substance:
E. all of the above A. assay
B. bioavailability
291. It refers to either prohibited or regulated drugs C. bioequivalence
which require a special prescriptions form: D. Physico-chemical test
A. ethical drugs E. extraction
B. OTC drugs
C. prescription drugs 298. Any device not used in health care but has been
D. dangerous drugs determined by the FDA to adversely affect the health
E. controlled precursors of the people:
A. health device
292. RA 9275 was signed into law on: B. medical device
A. June 7, 2002 C. Radiation device
B. February 26, 2004 D. contraceptive device
C. June 23, 1969 E. health- related device
D. June 22, 1963
E. February 24, 2006 299. It is the rate and extent to which the active
ingredient or therapeutic ingredient is absorbed from
293. R.A. 3720 was signed into law on: a drug and becomes available at the site of drug
A. June 7, 2002 action:
B. February 26, 2004 A. assay
C. June 23, 1969 B. bioavailability
D. June 22, 1963 C. radiation device
E. February 24, 1962 D. Physico-chemical test
E. none of the above
294. R.A. 7394 was signed into law on:
A. April 13, 1992 300. It is the branch of moral science that treats of the
B. February 26, 1992 obligations which a member of a profession owes to
C. February 7, 1992 the public, to HIS profession and to his clients
D. September 13, 1988 A. professional ethics
E. June 22, 1963 B. bioethics
C. ethics
295. R.A. 6675 was signed into law on: D. Non maleficence
A. April 13, 1992 E. none of the above
B. February 26, 1992