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India Generics 181813
India Generics 181813
Generics in India
July 2023
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1. Executive Summary
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TABLE OF CONTENTS
1. Executive Summary 2
2. Market Overview 8
3. Market Data 10
4. Market Segmentation 12
5. Market Outlook 13
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7. Competitive Landscape 23
7.3. Have there been any recent developments in the market? ......................................................................24
8. Company Profiles 26
9. Macroeconomic Indicators 40
9.2. Methodology..............................................................................................................................................42
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LIST OF TABLES
Table 1: India generics market value: $ million, 2017–22 10
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LIST OF FIGURES
Figure 1: India generics market value: $ million, 2017–22 10
Figure 9: Factors influencing the likelihood of new entrants in the generics market in India, 2022 19
Figure 10: Factors influencing the threat of substitutes in the generics market in India, 2022 20
Figure 11: Drivers of degree of rivalry in the generics market in India, 2022 21
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2. Market Overview
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In 2022, the Indian generics market witnessed an annual growth of 9%. The country has in place “Pradhan Mantri
Bhartiya Janaushadhi Pariyojana (PMBJP) responsible for the distribution of generic medicines at affordable prices
through outlets known as “Janaushadhi Kendras”. As of March 2023, the country has 9,303 Janaushadi Kendras.
The expanding distribution network for generics is supporting the market growth.
Market consumption volume increased with a CAGR of 0.4% between 2017 and 2022, to reach a total of 97.4% in
2022. The market's volume is expected to rise to 98.1% by the end of 2027, representing a CAGR of 0.1% over
2022–27.
The generic medication market is expanding due to its lower cost than patented original medications, giving them
an edge in volume-based procurement settings where there is intense price rivalry. Moreover, the country has a
large low-income population who cannot afford expensive medications. As a result, the Pharma & Medical Bureau
of India (PMBI) creates awareness through education and advertising about the quality of generic medications to
dispel the myth that quality is exclusively associated with high prices, hence supporting market growth.
The performance of the market is forecast to accelerate, with an anticipated CAGR of 8.4% over 2022–27, which is
expected to drive the market to a value of $26.3 billion by the end of 2027. Comparatively, the South Korean and
Chinese markets will grow with CAGRs of 4.8% and 8.9%, respectively, over the same period to reach respective
values of $6.6 billion and $171.1 billion in 2027.
The government of the country is also taking initiatives to promote the consumption of generic medicine across
the country. In May 2023, the Indian health ministry issued a notice asking doctors in the Central Government
Hospitals/CGHS Wellness Centers/Polyclinics to prescribe generic medicines only. Additionally, the National
Medical Commission Act, 2019, gives the State Medical Council and the Commission's Ethics and Medical
Registration Board (EMRB) the authority to take action against a doctor disobeying the regulations. Also, continued
investment in awareness campaigns for generic medicines and similar initiatives will continue to elevate demand.
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3. Market Data
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Year % % Growth
2017 95.5
2018 96.5 1.1%
2019 96.6 0.1%
2020 97.0 0.4%
2021 97.2 0.2%
2022 97.4 0.2%
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4. Market Segmentation
Geography 2022 %
China 111,666.9 68.8
India 17,617.5 10.8
Japan 14,960.2 9.2
South Korea 5,172.0 3.2
Taiwan 2,354.1 1.4
Rest of Asia-Pacific 10,611.6 6.5
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5. Market Outlook
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Year % % Growth
2022 97.4 0.2%
2023 97.7 0.2%
2024 97.8 0.1%
2025 97.9 0.1%
2026 98.0 0.1%
2027 98.1 0.1%
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6.1. Summary
Rivalry in the Indian generics market is strong. Without very much product differentiation, or the brand loyalty enjoyed
by some branded drugs, the main players engage in price wars. High fixed costs and exit costs add to this rivalry and, as
a result, players tend to be large and have a good deal of expertise in the market.
Buyers can easily switch between manufacturers of generics and decisions are very likely to be price based.
Governments can have a heavy influence on how generics are sold and how they are prioritized in the healthcare
system.
Suppliers of APIs (active pharmaceutical ingredients) are largely similar companies to the players, so integration is very
likely. However, packaging companies tend to be independent and have various revenue streams, so they are less likely
to rely on the generics market.
Although the products have to be biosimilar to the original drug to gain status as a generic, the entry barriers are lower
than for a patented new drug, which means that new entrants are likely. Patented drugs producers already have the
capabilities to enter the market and there tends to be much M&A activity in the market.
The original drug will always be a substitute for the generic for more brand-oriented consumers. In addition, non-
medicinal therapy and alternative medicine are other options that may be considered.
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Buyers can range from small companies to large corporate entities, such as healthcare facilities and large retailers.
These different buyers experience varying levels of buyer power. India’s national health insurance, Rashtriya Swasthya
Bima Yojana (RSBY), and large private companies such as Fortis Healthcare, have strong financial muscle as the volume
of orders placed is likely to be high and any loss of business would have a large financial impact on players in the market
which increases buyer power. However, the large number of available buyers decreases the buyer power because
players do not have to rely on a finite number of buyers, even if there are some which are much more valuable than
others.
Except for OTC (over-the-counter) and similar drugs, prescriptions are generally required to obtain pharmaceutical
products. The marketing of prescription drugs by their manufacturers is therefore largely directed at medical
practitioners, with whom they wield significant influence. Marketing directly to consumers is illegal in most countries,
including India.
There is little brand awareness associated with generics and the products are, by definition, very similar to the original
previously patented drug, so switching costs are low and buyers can usually choose the cheapest option. Paracetamol
(Acetaminophen), for example, is manufactured by hundreds of companies but the product itself must stay largely the
same apart from its packaging and appearance, which companies are free to change.
Switching costs are negligible for individuals because they are likely to only be purchasing a small amount, so can
choose freely from the available choices, but contracts can increase switching costs for buyers that buy in bulk.
Medication for life-threatening diseases is indispensable to patients and healthcare facilities, but patients may choose
not to pay for treatment or try alternative therapies if symptoms are milder. They may also choose a non-generic if they
are more brand focused. Buyers are unlikely to backward integrate into generics manufacturing which reduces buyer
power. However, players are fully independent of their buyers as their business set-ups are very different and cannot
integrate forward, which increases buyer power.
Overall, buyer power in the generics market is strong.
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The main suppliers to this market are manufacturers of active pharmaceutical ingredients (APIs) and packaging
suppliers. Packaging suppliers are largely independent of players and have an array of different customers across many
industries, so they do not need to rely on the generics market for revenue which increases their power. However,
packaging suppliers have comparatively lower power as generic manufacturers can use different types of packaging
because appearance is not very important to end users and the quality of the packaging is much less important than the
actual ingredients in the drug. API manufacturers, however, have a large reliance on pharmaceutical companies for
their revenue. The country relies heavily on the import of APIs to manufacture pharmaceutical goods and meet rising
demand. In response, the Indian government announced a Production Linked Incentive Scheme (PLI) for
pharmaceutical drugs in March 2021. The scheme focuses on the promotion of domestic manufacturing of key starting
materials (KSMs), drug intermediates (DIs), and APIs. Under the scheme, the government will invest in new machinery
and equipment, research facilities, and the building of new production plants. A greater number of API suppliers could
weaken supplier power as pharmaceutical companies are not reliant on a limited number of suppliers for key raw
manufacturing materials.
Players also have a huge reliance on the suppliers to provide high-quality APIs, without any substitute inputs to fall back
on. As a result of this close dependence, large generic companies are likely to backward integrate into producing APIs
themselves, reducing supplier power. However, suppliers are also very likely to forward integrate into generics if they
have the chemical synthesis know-how.
Pharmaceutical companies enter into contractual agreements with suppliers to secure enough supplies to maintain
their large orders, and they may therefore incur switching costs if they decide to change suppliers. This gives the
suppliers increased power over market players. Alternatively, pharmaceutical companies employ sourcing managers to
minimize costs when purchasing APIs.
Market players tend to purchase their raw materials from numerous suppliers, reducing their reliance on any particular
company. In general, laboratory equipment and chemicals show little differentiation between suppliers, with players
utilizing a high degree of choice to obtain the best quality and cost relationship, reducing supplier power. However,
there are instances where specialized facilities or raw materials are required, such as the sterile processing of biological
materials. In such cases, supplier power is much stronger.
It is unlikely that suppliers would forward-integrate into the pharmaceuticals market; however, their capabilities in
chemical synthesis make them ideal candidates for forward integration into the manufacture of generic drugs. Several
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players can integrate backward into chemical manufacturing, providing them with a degree of self-sufficiency, and
reducing supplier power.
It is common for pharmaceutical companies to outsource drug testing and clinical trials to third-party test service
providers. Given the importance of these trials for regulatory approvals, these service providers are also important
suppliers. COVID-19 has highlighted issues with supply chains, with most APIs sourced from countries such as India and
China. Firms often use one plant for supply, an issue that has been exposed due to regional lockdowns causing
significant disruption. Diversifying the supply chain, so as not to be left stranded in the event of a crisis, is likely to be a
change in the coming years.
Overall, supplier power in the generics market is strong.
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Figure 9: Factors influencing the likelihood of new entrants in the generics market in India, 2022
Entry barriers are typically lower in this market than those in the wider pharmaceutical industry. However, the existing
players in the generics market such as SunPharma and Lupin, as well as domestic company Aurobindo benefit from
scale economies, and the new players are expected to compete with these incumbents, boosting entry barriers. There
are also high costs incurred when setting up production facilities and employing highly trained staff. Also, barriers to
entry for a generics company will depend on factors such as the expiry of patents on those drugs it intends to replicate
and the likelihood that the patent holder will protect its market position by offering a similar drug under a new or
extended patent.
The generics market is highly regulated by the government to ensure the quality and safety of the drug. In India, Central
Drugs Standard Control Organization (CDSCO) authorizes companies to produce generic medicines. Generic
manufacturers must adhere to stringent manufacturing practices and quality control standards and ensure that the
active substance of generic medicine is similar to the original product. These regulations restrict new entrants in the
industry. Recently, the US FDA tightened stringent regulatory rules for Indian pharmaceutical companies producing
generic drugs through an increase in inspections and Open Access Initiatives (OAI) at Indian sites.
The easy access to distribution channels encourages the entry of new players in the market. The manufacturers can
either offer their products through online pharma retails or through offline stores. The convenience, flexibility, and
comfort offered by online channels are encouraging its popularity. For instance, Medkart, PharmEasy, and Netmeds are
some of the popular online pharmacies in the Indian market.
Due to the uncertainty brought about by the COVID-19 pandemic in 2020, any potential new entrants are likely to have
been deterred that year. The generic and pharmaceutical markets were hit with supply chain disruptions in the
production of APIs at the early stages of the outbreak, which made it more challenging for any new players to enter the
market and begin producing generic products. However, as supply chains recovered and demand stabilized in 2021 and
2022, the market is expected to become more attractive to new entrants.
Overall, the likelihood of new entrants can be assessed as moderate.
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Figure 10: Factors influencing the threat of substitutes in the generics market in India, 2022
Patented drugs are the main substitutes to the generics market. Typically, a generic is only produced after a patent has
expired, which can be up to 20 years after original production. This gives producers of patented drugs time to develop a
new therapeutic agent which might be more effective and, therefore, more attractive to clinicians and consumers than
a generic product. Patented drugs are almost always more expensive than generic drugs because the original producers
need to fund research into the next generation of medications. However, generics must be approved as an equivalent
to the original drug, so there is no clinical benefit to choosing a patented drug over a generic.
Where mental illness, such as anxiety or depression, is concerned, cognitive behavioral therapy is a substitute. Recent
years have seen something of a backlash against a perceived overuse of pharmaceuticals to treat patients suffering
from such illnesses and cognitive behavioral therapy is therefore a significant substitute.
Over recent years, the use of holistic therapies by the general public has grown. Holistic therapies are inexpensive, but
lack rigorous clinical testing, making their alleged therapeutic benefits questionable. Ayurvedic medicine is one of the
oldest systems of medicine in the world and has been practiced in India for thousands of years. It combines diet,
exercise, and herbal remedies and its research is supported by the Indian government. Most Indians will use some sort
of Ayurvedic therapy exclusively or alongside generic medication.
Overall, the threat of substitutes to this market is moderate.
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Figure 11: Drivers of degree of rivalry in the generics market in India, 2022
The Indian generics market consists of numerous players such as Sun Pharma, Lupin, Aurobindo Pharma, and Cipla. The
industry is highly competitive due to the large size of players. Leading incumbents within this market are typically
multinational companies that have a large geographical presence which eases rivalry. India, however, is dominated by
large local players, which increases rivalry. Lupin has acquired pharmaceutical companies in Russia, South Africa, Brazil,
Germany, and the US, which means it doesn't have to rely on India's generics market alone.
The capital-intensive nature of the industry increases the competitive rivalry between the players. The industry also
involves high exit barriers due to large capital investment, compelling players to operate even at lower margins, and
increasing the rivalry. The players focus on stringent quality and safety management principles to ensure the delivery of
quality products to their clientele to retain customers. Compliance with quality standards builds the company’s brand
image and boosts the customer’s confidence in the player.
The ability of generics companies to be profitable while selling the same molecule at a much lower price than the
originator, following patent expiration, shows that establishing high-quality manufacturing processes is not prohibitively
costly. A secondary effect of this is that it is relatively easy for companies to expand output, for example, through
licensing agreements with other companies, without the need to scale up their production facilities. Given the
increasing linkages between regulatory authorities and the greater likelihood of a drug being approved in multiple
locations, this tends to boost rivalry.
It is moderately easy to exit the generics market. The lack of patents means that there is little IP to protect, unlike in the
wider pharmaceutical industry. Many of the R&D and production facilities and equipment will have uses outside
pharmaceutical research or manufacture.
Some of the largest pharmaceutical companies have their own generics branch, such as Novartis, which owns Sandoz.
These types of companies will have the expertise and reputation of parent companies, which could give them a
competitive edge over those who work in generics alone. There is also the benefit of protection from a declining
generics market. As products are largely undifferentiated, once companies are established, it is easy to expand into
other kinds of generics, and the rivalry increases.
There is little brand loyalty in this market and switching products is unlikely to incur a cost for buyers unless a contract
is involved, which means that companies must embark upon competitive pricing strategies to ensure a strong customer
base.
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The market witnessed strong growth during the historic period due to the expanding outsourcing of manufacturing to
India due to lower production costs, which eased rivalry. Moreover, the acceleration of market growth over the
forecast period is expected to further ease rivalry among the players.
Overall, the degree of rivalry is assessed as strong.
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7. Competitive Landscape
The Indian generics market has been experiencing rapid growth for a long time now. Value growth has continued
to be strong even though generics’ share of pharmaceuticals is high. This is largely due to rising wages and a
burgeoning middle class that is paying greater attention to healthcare. The market is dominated by domestic
players, which have experienced strong growth in recent years due to increasing demand for generics. The Indian
generics market consists of four main leaders: Sun Pharma, Lupin, Aurobindo Pharma, and Cipla.
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sells its products in more than 100 countries in emerging markets, including Latin America, Africa, Asia, and
Eastern & Central Europe. It has a strong R&D division that focuses on the development of a strong product
pipeline for sustainable growth. In FY2022, the company incurred R&D expenses of INR22.1 billion ($281.5 million),
which as a percentage of revenue, stood at 5.8%. The company's research expertise spans the development of
generics, active pharmaceutical ingredients (API), and novel drug delivery systems (NDDS). As of March 31, 2022,
the company had 512 approved Abbreviated New Drug Applications (ANDAs) and 605 filed ANDAs.
Lupin is an innovation-led transactional pharmaceutical company producing a wide range of quality, affordable
generic and branded formulations, and APIs. The company is one of the largest and fastest-growing generic
pharmaceuticals in India. As on March 31, 2023, the Company has 28 subsidiaries and a joint venture. Lupin
markets its drugs and products in over 100 countries worldwide. The company has a strong portfolio of products
including 463 ANDAs and four NDAs which have been approved by the US FDA. It has 17 ANDAs approved and 28
filed and three NDAs approved and three filed. A strong portfolio of generic products enables Lupin to serve
diversified end markets that hold attractive long-term growth characteristics. Some of its leading products include
Rifapentine, Rifabutin, Rifampicin, Pyrazinamide, and Ethambutol, as well as products in cephalosporins including
cephalexin and their intermediates.
Aurobindo is a vertically integrated pharmaceutical company that delivers novel solutions. It provides drug
development and substantial manufacturing services from discovery to development to commercialization. This
includes complete R&D to identify and advance substances for further development and improve manufacturing
facilities, sales, and marketing operations. The company’s operations from conception to commercialization
provide several advantages, such as reduced manufacturing and delivery times, lower costs, direct sourcing of raw
materials, and quality control for each of its divisions. Approximately 70% of the company’s API requirement is
being met in-house. The company is also focused on vertically integrating the manufacturing plants for most
generic formulations, to ensure timely material availability and operations, and to decrease the dependency on
import of APIs and intermediaries. The company has 14 manufacturing formulations facilities, 10 API plants, and
packaging facilities worldwide.
Cipla has a strong foothold in the Indian market and has a wide product portfolio. It offers over 1,500 and above
products across 86 countries in 65 therapeutic categories and over 50 dosage forms. The company has strong R&D
capabilities. As of March 2022, it had five R&D units. Additionally, it had 269 cumulative ANDAs/NDAs and 278
awarded patents. In addition to having specialized cancer and polypeptide development labs, Cipla managed five
research sites for the development of API processes in India. The company spent INR11.2 billion ($142.8 million)
on R&D in FY2022, which amounted to 5.2% of total revenue.
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Eugia Pharma Specialities is a company engaged in developing, manufacturing, and marketing hormonal and
oncology generic formulations. Through this acquisition, both Eugia Pharma Specialities and MViyeS Pharma
Ventures have become 100% subsidiaries of Aurobindo, which has helped the latter widen its product portfolio.
In June 2021, Dr. Reddy’s completed the acquisition of select divisions of generics businesses in India and a few
other international territories (Nepal, Sri Lanka, Bhutan, and the Maldives) from Wockhardt, a pharmaceutical and
biotechnology company. The business comprises a portfolio of 62 brands in multiple therapy areas, such as
respiratory, neurology, VMS, dermatology, gastroenterology, pain, and vaccines, which have transferred to Dr.
Reddy’s, along with the related sales and marketing teams. This also includes the manufacturing plant located in
Baddi, Himachal Pradesh, with all plant employees. The acquisition is in line with Dr. Reddy’s strategic focus on
India and has paved the way for accelerated growth and a better position in the domestic market.
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8. Company Profiles
Sun Pharmaceutical Industries Ltd (Sun Pharma) is a specialty pharmaceutical company that offers a wide range
of pharmaceutical formulations such as branded generics and generic pharmaceuticals. The company’s
portfolio includes products for the treatment of psychiatric, neurological, nephrological, gastroenterological,
orthopedic and ophthalmologic diseases and disorders, and heart diseases. The company carries out product
development, process chemistry, and manufacture of complex formulations, active pharmaceutical ingredients
(APIs) and over-the-counter products. It offers drugs in various dosage forms such as tablets, capsules,
injectables, inhalers, ointments, creams, and liquids. The company has manufacturing facilities in North
America, Latin America, EMEA and Asia Pacific. Sun Pharma is headquartered in Mumbai, Maharashtra, India.
The company reported revenues of (Rupee) INR438,856.8 million for the fiscal year ended March 2023
(FY2023), an increase of 13.5% over FY2022. In FY2023, the company’s operating margin was 20.7%, compared
to an operating margin of 8.4% in FY2022. In FY2023, the company recorded a net margin of 19.3%, compared
to a net margin of 8.5% in FY2022.
Head office: Sun House Cts No. 201 B/1, Western Exp, , Mumbai, Maharashtra, India
Telephone: 912243244324
Fax: 9123244343
Number of Employees: 38000
Website: sunpharma.com
Financial year-end: March
Ticker: SUNPHARMA
Stock exchange: National Stock Exchange of India
Source: COMPANY WEBSITE MARKETLINE
Sun Pharmaceutical Industries Ltd (Sun Pharma) manufactures and supplies more than 400 generic (branded and
non-branded) pharmaceuticals to treat conditions such as diabetes, central nervous system disorders, central
vascular system disorders, and respiratory and infectious diseases. The company markets these drugs in various
dosage forms such as tablets/capsules, semi-solids, liquids and suppositories. It has a portfolio of more than 2,000
marketed products. It manufactures more than 370 APIs, which include a number of APIs with regulated market
approval such as US and European drug master files (DMFs).
Sun Pharma classifies its business into three categories namely, Formulations, API, and Others. The company’s
Consumer Healthcare (CHC) business division develops and markets over-the-counter (OTC) products in India.
It operates 43 manufacturing facilities for formulations and APIs. Formulations units are located as 15 in India,
three in the US, two in Japan and one each in Russia, Canada, Hungary, Bangladesh, Israel, Romania, South Africa,
Nigeria and Malaysia while 14 API facilities spread across various countries. It operates in more than 100 countries
in emerging markets, including across Latin America, Africa, Asia and Eastern & Central Europe.
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Lupin Ltd (Lupin) develops and manufactures generic and branded formulations, biotechnology products, and
active pharmaceutical ingredients (APIs). It has expertise in the areas of cardiovascular, asthma, diabetic
management, pediatrics, central nervous system, gastro-intestinal, anti-infectives, nonsteroidal anti-
inflammatory drugs (NSAIDs), anti-TB, and cephalosporins. The company undertakes extensive research and
development activities of pharmaceuticals for the treatment of migraine, gastrointestinal, psoriasis, central
nervous system, cardiovascular, diabetes, tuberculosis, inflammation and others. Lupin also develops value-
added generic pharmaceuticals based on its platform technologies. The company along with its subsidiaries
operates manufacturing facilities in India, the US, Mexico, and Brazil. Lupin is headquartered in Mumbai,
Maharashtra, India.
The company reported revenues of (Rupee) INR166,416.6 million for the fiscal year ended March 2023
(FY2023), an increase of 1.4% over FY2022. The operating profit of the company was INR8,814.6 million in
FY2023, compared to an operating loss of INR13,939.9 million in FY2022. The net profit of the company was
INR4,300.8 million in FY2023, compared to a net loss of INR15,280.4 million in FY2022.
Head office: B/4 Laxmi Towers Bandra Kurla Complex, Bandra (E), Mumbai, Maharashtra, India
Telephone: 912266402222
Fax: 912266402130
Number of Employees: 18971
Website: www.lupin.com
Financial year-end: March
Ticker: LUPIN
Stock exchange: National Stock Exchange of India
Source: COMPANY WEBSITE MARKETLINE
Lupin Ltd (Lupin) undertakes the manufacture and marketing of generic and branded pharmaceutical products,
and active pharmaceutical ingredients (APIs). The company focuses on therapeutic areas such as generics,
biosimilars, specialty, over-the-counter, active pharmaceutical ingredients, global institutional business, tech-
driven offerings. It is one of the leading and fasting growing companies.
Its product portfolio is focused on various therapeutic areas such as cardiovascular, diabetics, asthma, respiratory
diseases, pediatrics, oncology, immunology, metabolic disorders, central nervous system, gastrointestinal,
tuberculosis, infections and non-steroidal anti-inflammatory drugs. The company is also focused on oral,
ophthalmic, dermatology and inhalation product development. The company reports its operations under single
segment, namely, Pharmaceuticals. Lupin’s business includes formulations, active pharmaceutical ingredients
(APIs), generic formulations, and biotechnology products. The company has eight major brands including
Gluconorm-G, Budamate, Ivabrad, Ajaduo, Tonact, Ondero and Rablet-D. The business operates 15 global
manufacturing facilities worldwide. Its APIs products include antibiotics for cephalosporin and non-systemic
gastro-intestinal; Anti-B; cardiovascular products including anti-hypertensive, anti-hyperlipidemic and anti-
thrombotic, for CNS including anti-convulsant, anti-Parkinson and neuropathic pain agent; as well as for analgesics
and anti-gout. The company's biotechnology (biotech) division focuses on manufacturing high quality biologics and
biosimilars.
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It is developing biosimilar for Etanercept under the brand Enbrel. Lupin’s advanced drug delivery systems business
has developed various platforms including, bio-adhesive / gastro-retentive extended release systems, laser-drilled
extended release systems, bioavailability enhancement systems based on solubilization and nano-particle
technology, matrix or reservoir based release systems, and taste masking technologies for solid and liquid orals.
The company operates manufacturing facilities in India: Aurangabad, Ankleshwar, Dabhasa, Goa, Pithampur,
Jammu, Mandideep, Nagpur, Pune, Sikkim, Tarapur & Vizag U.S; New Jersey; LATAM: Mexico & Brazil. It marketed
the business in Australia, Brazil, Canada, Mexico, the Philippines, and South Africa. Geographically, the company
generates its revenue from three regions, namely, India, the United States, and other. In FY2023, the company's
capital expenditure stood at INR14996.2 million
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Aurobindo Pharma Ltd (Aurobindo) is a vertically integrated pharmaceutical company that manufactures and
markets generic pharmaceuticals and active pharmaceutical ingredients (APIs). Its product portfolio is spread
across major therapeutic and product categories including antibiotics, anti-retroviral, systemic
gastroenterological, central nervous system, cardiovascular, anti-allergies, anti-diabetics, other therapeutic
areas. The company also produces novel proprietary biocatalysts, vitamins, minerals, dietary supplements,
sports nutrition, functional foods, weight loss products and fermentation-based semi-synthetic products.
Aurobindo operates manufacturing facilities in India, Brazil, Portugal and the US; and R&D, facilities in India and
the US. The company exports products to several countries worldwide. Aurobindo is headquartered in
Hyderabad, Telangana, India.
The company reported revenues of (Rupee) INR248,553.8 million for the fiscal year ended March 2023
(FY2023), an increase of 6% over FY2022. In FY2023, the company’s operating margin was 10.1%, compared to
an operating margin of 13% in FY2022. In FY2023, the company recorded a net margin of 7.8%, compared to a
net margin of 11.3% in FY2022.
Aurobindo Pharma Ltd (Aurobindo) is a global pharmaceutical company that manufactures generic formulations,
active pharmaceutical ingredients (APIs) and specialty products. The company’s product portfolio is spread over
seven key therapeutic areas, including antibiotics antiretrovirals (ARVs), cardiovascular, central nervous systems
(CNS), anti-diabetics, gastro-enterologicals, and anti-infectives.
It offers a broad portfolio of diversified dosage forms, including prescription and OTC oral solids and liquids,
specialty products such as ophthalmics, injectables and controlled substances in generic formulations. The
company also provides customer centric project-based chemistry services and stability study activities through
AuroSource; novel solutions from discovery to development and commercialization to cost-effective drug
development and manufacturing through Auro Peptides Ltd; and biocatalysts for use in the pharmaceutical and
chemical Industries through AuroZymes.
The company operates through various reportable segment. Its business operations consist of manufacturing and
selling US Formulations, EU Formulations, Growth Markets Formulations, ARV formulations and API business
segment. It markets products and solutions in more than 150 countries. The company has several manufacturing
facilities for APIs-oral and sterile, drug intermediates and formulations. It operates 11 units for APIs/intermediates
and 15 units, including 10 in India, 3 in the US and 1 each in Portugal and Brazil) for formulations.
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Cipla Limited (Cipla or 'the company') is a manufacturer of prescription drugs, veterinary and active
pharmaceutical ingredient products. The company provides products for various therapeutic categories
including dermatology, critical care, cardiovascular, infectious diseases, children's health, and cosmetology,
HIV/AIDS, diabetes, neurosciences, hepatitis, malaria, oncology, ophthalmology, respiratory, osteoporosis and
urology. It also manufactures metered-dose inhaler devices, spacers and related devices. Cipla is engaged in
biosimilar and consumer healthcare. Cipla operates manufacturing facilities in multiple locations across the
world. Cipla offers its products in South Africa, India, and North America and other markets. The company is
headquartered in Mumbai, Maharashtra, India.
The company reported revenues of (Rupee) INR227,531.2 million for the fiscal year ended March 2023
(FY2023), an increase of 4.5% over FY2022. In FY2023, the company’s operating margin was 16.3%, compared
to an operating margin of 15.3% in FY2022. In FY2023, the company recorded a net margin of 12.3%, compared
to a net margin of 11.6% in FY2022.
Cipla Limited (Cipla or ‘the company’) develops, manufactures, and sells pharmaceutical products. It has over
1,500 and above products across 86 countries in 65 therapeutic categories and over 50 dosage forms.
The company operates through two business segments: Pharmaceutical and New Ventures.
Under Pharmaceuticals segment, the company develops, manufactures, sells and distributes generic and branded
medicines. It also produces active pharmaceutical ingredients (APIs) which manufactures more than 200 generic
and complex APIs. The portfolio covers a range of therapeutic categories including urology, oncology, cardio-
metabolism, child health, infectious diseases & critical care, hepatitis, women’s health, ophthalmology, neuro –
psychiatry, respiratory, asthma, paediatric asthma, COPD, nebulization, and HIV/AIDS. In FY2022, the
Pharmaceuticals segment generated revenue of INR213,512.7 million, which accounted for 97.6% of the
company’s revenue.
Under New Ventures segment include the operations of consumer healthcare, biosimilars and specialty business. It
operates through Cipla BioTec Pvt Ltd (Cipla BioTec), which is involved in the development and research activities,
producing and developing and distributing Cipla Health Ltd (Cipla Health), a consumer healthcare company and
biosimilars. The segment formed CipTec for specialty business in the US. In FY2022, the New Ventures segment
generated revenue of INR5,315.1 million, which accounted for 2.4% of the company’s revenue.
Industry Profiles
Geographically, Cipla classifies its operations into four reportable segments: India, the US, South Africa, and Rest of
the World. Cipla has its presence in Australia, Europe, Kenya, Malaysia, Morocco, Nepal, South Africa, Spain, Sri
Lanka, Uganda, United Kingdom and the US. As of March 2022, the company operated 47 manufacturing facilities
across six countries and 33 regulatory inspections. It also operated 38 national and nine international plants. In
FY2022, India accounted for 45.2% of its total revenue followed by 20.4% from US, 12.1% from South Africa and
22.4% from Rest of the World.
Industry Profiles
Industry Profiles
Industry Profiles
9. Macroeconomic Indicators
Industry Profiles
Industry Profiles
Appendix
9.2. Methodology
MarketLine Industry Profiles draw on extensive primary and secondary research, all aggregated, analyzed, cross-
checked and presented in a consistent and accessible style.
Review of in-house databases – Created using 250,000+ industry interviews and consumer surveys and supported by
analysis from industry experts using highly complex modeling & forecasting tools, MarketLine’s in-house databases
provide the foundation for all related industry profiles
Preparatory research – We also maintain extensive in-house databases of news, analyst commentary, company profiles
and macroeconomic & demographic information, which enable our researchers to build an accurate market overview
Definitions – Market definitions are standardized to allow comparison from country to country. The parameters of each
definition are carefully reviewed at the start of the research process to ensure they match the requirements of both the
market and our clients
Extensive secondary research activities ensure we are always fully up-to-date with the latest industry events and trends
MarketLine aggregates and analyzes a number of secondary information sources, including:
- National/Governmental statistics
- International data (official international sources)
- National and International trade associations
- Broker and analyst reports
- Company Annual Reports
- Business information libraries and databases
Modeling & forecasting tools – MarketLine has developed powerful tools that allow quantitative and qualitative data to
be combined with related macroeconomic and demographic drivers to create market models and forecasts, which can
then be refined according to specific competitive, regulatory and demand-related factors
Continuous quality control ensures that our processes and profiles remain focused, accurate and up-to-date
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Tel.: 91 22 2494 4624
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Global Generics
Generics in Europe
Generics in Asia-Pacific
Generics in Japan
Generics in China
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