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Pharmaceuticals in India May 2020: Marketline Industry Profile
Pharmaceuticals in India May 2020: Marketline Industry Profile
Pharmaceuticals in India
May 2020
WWW.MARKETLINE.COM
MARKETLINE. THIS PROFILE IS A LICENSED PRODUCT
AND IS NOT TO BE PHOTOCOPIED
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1. Executive Summary
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TABLE OF CONTENTS
1. Executive Summary 2
2. Market Overview 7
3. Market Data 9
4. Market Segmentation 10
5. Market Outlook 11
7. Competitive Landscape 22
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7.5. What has been the rationale behind recent M&A activity? .........................................................24
8. Company Profiles 25
9. Macroeconomic Indicators 40
Appendix 42
Methodology............................................................................................................................................ 42
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LIST OF TABLES
Table 1: India pharmaceuticals market value: $ billion, 2015–19 9
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LIST OF FIGURES
Figure 1: India pharmaceuticals market value: $ billion, 2015–19 9
Figure 7: Factors influencing the likelihood of new entrants in the pharmaceuticals market in India, 201917
Figure 8: Factors influencing the threat of substitutes in the pharmaceuticals market in India, 2019 19
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2. Market Overview
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The Indian pharmaceuticals market declined by 7.4% in 2016, but the market achieved healthy growth rates of around
5% for the remainder of the historic period. The market is expected to decelerate in the forecast period, with
moderate rates expected overall.
The Indian market is growing, driven by an increase in real GDP, doctors and India’s population covered by insurance.
A number of major government initiatives are set to support this growth in the future. In October 2018, the
government announced it will create six pharma science parks and has received more than $712–855m in private
investment for six more. In the 2018–2019 budget, the government announced the National Health Protection
Scheme, the largest government funded healthcare programme in the world. This scheme is expected to benefit 100m
poor families in the country by providing health insurance cover for secondary and tertiary care.
The Indian pharmaceuticals market had total revenues of $32,500.0m in 2019, representing a compound annual
growth rate (CAGR) of 2.2% between 2015 and 2019. In comparison, the South Korean and Chinese markets grew with
CAGRs of 5.2% and 8% respectively, over the same period, to reach respective values of $19,636.6m and $142,557.2m
in 2019.
The Indian market supplies around 40% of generic demand in the US and 25% of all medicine in the UK. Around 80%
of the world’s antiretroviral drugs used in the treatment of HIV/AIDs are made in India. The cost of manufacturing
formulations in India remained 30–40% lower than other comparative manufacturing hubs such as China and Eastern
Europe. India is a major exporter, and although half the revenues of its pharmaceutical market come from exports,
due to their superior profitability compared to domestic products, they contribute much more to net income within
the country.
The government has recently announced plans to consolidate approvals and regulatory practices onto a single ‘portal’,
emphasising its Made in India initiative. Further, it has unveiled its 'Pharma Vision 2020', aimed at making India a
global leader in end-to-end drug manufacture. Additionally, India offers several advantages that make it a preferred
R&D destination for biotechnology research. As of 2019, of all the 3,895 US Food and Drug Administration approved
manufacturing plants outside the US territory, 729 are situated in India, with a global share of 18.72%. Over 300
Indian colleges specialize in bioinformatics and the biological sciences, and produce over 500,000 graduates annually,
highlighting the country’s strengths as a pharmaceutical hub.
Domestic demand for pharmaceutical products is being driven by demographic changes within the country. India has
an aging population. A report released by the United Nations Population Fund and HelpAge India suggests that the
number of elderly persons is expected to grow to 173 million by 2026. Furthermore, there is a rising incidence of
chronic diseases such as diabetes and weight-associated cardiovascular disease as the prevalence of overweight and
obesity has increased rapidly in recent decades. This has and will continue to drive demand for pharmaceutical
products within the country.
The performance of the market is forecast to accelerate, with an anticipated CAGR of 3.5% for the five-year period
2019-2024, which is expected to drive the market to a value of $38,554.5m by the end of 2024. Comparatively, the
South Korean and Chinese markets will grow with CAGRs of 3.9% and 7.7% respectively, over the same period, to
reach respective values of $23,822.0m and $206,279.4m in 2024.
At the time of writing it is difficult to predict how the market will perform in the coming years due to the widespread
outbreak of COVID-19; however, its impact on the Indian pharmaceuticals market is expected to be minimal, with
moderate growth still expected in 2020. Indian manufacturers rely heavily on APIs from China for the production of
their pharmaceuticals, therefore the closure of manufacturing in China has caused supply chain disruptions. This is
expected to lead to a slowdown in growth in 2020. However, pharmaceuticals are a necessity and demand is unlikely
to change much.
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3. Market Data
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4. Market Segmentation
Geography 2019 %
China 142.6 46.6
Japan 59.3 19.4
India 32.5 10.6
South Korea 19.6 6.4
Taiwan 2.5 0.8
Rest Of Asia-pacific 49.3 16.1
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5. Market Outlook
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6.1. Summary
Figure 4: Forces driving competition in the pharmaceuticals market in India, 2019
The presence of large scale competitors and smaller generics companies fighting for each drug approval in a lucrative
market ensures rivalry is strong. Strong growth is helping to alleviate the rivalry in the Indian market.
The pharmaceuticals market is characterized by fairly strong buyer power, with the ease of market entry strongly
affected by legal and regulatory frameworks.
India has healthcare insurance offered by the state-owned General Insurance Company (GIC) and its subsidiaries.
Private insurance is also available, although it is currently much less significant than the GIC schemes. However,
neither public nor private health insurance has high penetration in India, with much of the population lacking
coverage and 70% of health spending met by out-of-pocket private spending. There is also a divide between
healthcare provision for the affluent urban classes, and the poorer, rural communities.
Buyer power is strengthened by the oligopsony status and price control policies of state and private sector institutions
that are ultimately the purchasers of drugs. Obtaining high quality materials, equipment, personnel, and third-party
clinical testing services is vital to the business of pharmaceutical companies.
New entrants must satisfy regulators that their products are safe and effective. Non-drug therapies are substitutes for
many pharmaceuticals. In addition, research-based drugs that are no longer protected by patents may be substituted
by cheaper generic copies, with many 'blockbuster' drugs coming off patent in the next few years giving the market a
so-called 'patent-cliff' to negotiate.
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This risk is, however, mildly reduced, as not all drugs have an effective generic replacement, meaning the original is
able to be sold unhindered by competitors even after the patent ends. In some instances, it is even the original
company that produces the generic in order to try to prevent generic makers from muscling into the market.
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Pharmaceutical manufacturers may sell to drug wholesalers, which then sell on to pharmacies, or to healthcare
institutions such as hospitals. Developing markets such as India are becoming increasingly important for
manufacturers given the pricing pressures being applied in mature economies. Some of the largest buyers in the
Indian market include India’s national health insurance, Rashtriya Swasthya Bima Yojana (RSBY) and Fortis Healthcare,
which have strong financial muscle and purchase large quantities of drugs. Some independent pharmacies exist but
these often operate on a small scale and supply isolated communities.
Except for OTC and similar drugs, prescriptions are generally required in order to obtain pharmaceutical products.
Marketing of prescription drugs by their manufacturers is therefore largely directed at medical practitioners, with
whom they wield a significant influence. In fact, with the notable exception of the US, advertising such products
directly to consumers is usually illegal.
Depending on the medical condition, there may be several different drug treatments available and product
differentiation in these cases weakens buyer power. Such differentiation can include efficacy, ease of use, side effects,
and cost-effectiveness. The move towards genetic and genomic research, giving rise to the possibility of personalized
medicine, is also likely to decrease buyer power. Conversely, where generic equivalents to a branded drug exist,
differentiation is decreased and buyer power enhanced.
The primary source of funds for drug purchases is, in some cases, a public or private-sector health insurer or similar
body. These may fund purchases directly or they may reimburse some or all of an end-user’s initial purchase. This
increases buyer power. Not only can such large purchasers exert monopsony market power, but also it is very
common for them to use one or more specific price control strategies. The majority of funding in India, however,
comes from private out-of-pocket expenditure.
Governments may simply set drug prices directly, in which case it becomes illegal to sell at a different price. Where
governments are responsible for the reimbursement of consumers, they may set a very low reimbursement price for
new or existing drugs on the market.
India has healthcare insurance offered by the state-owned General Insurance Company (GIC) and its subsidiaries.
Private insurance is also available, although it is currently much less significant than the GIC schemes. However,
neither public nor private health insurance has high penetration in India, with much of the population lacking
coverage and 70% of health spending met by out-of-pocket private spending. There is also a divide between
healthcare provision for the affluent urban classes, and the poorer, rural communities.
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Reference price regimes, in which reimbursement levels are set, by comparison of the price of a drug in peer group
countries and/or therapeutic categories, are common. Where a therapeutic category contains generics, the effect may
be to push down the reference price for on-patent drugs in the same category. A similar effect can occur where peer
group countries have lower per capita incomes than the country making the comparison.
Price-volume or profit controls may exist. These set a limit to the volume of a drug which may be sold in the country,
or to the amount of profit a drug company can make, beyond which manufacturers must offer either compensatory
payments to the government or price reductions.
Such systems may be regarded as market distortions. However, where they are in force, it is because policy makers
consider that the social benefits of lower-cost drugs, such as improved access to healthcare, outweigh the social
harms, such as a potential reduction in pharmaceutical companies’ ability to invest in R&D.
The Indian government's National Pharmaceutical Pricing Authority exerts control over the price of a list of so-called
‘scheduled’ drugs. It also monitors price trends for other pharmaceuticals, and imposes a limit of 10% on annual price
increases. In February 2018, the Indian government announced it will be introducing major changes to the current
Drug Pricing Control Order (DPCO), which will be replaced with a new pharma policy to implement the National Health
Protection Scheme or ‘Namocare’ across the country. Namocare will be aimed at benefiting 10 crore poor families by
providing coverage of up to Rs5 lakh per family each year for secondary and tertiary healthcare. Buyer power has
increased in recent years due to rising healthcare costs and the increasing availability of generics.
Overall, buyer power is assessed as strong."
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Major suppliers to the pharmaceuticals market are manufacturers of active pharmaceutical ingredients (APIs), which
form a sub-sector of the chemical industry and produce key inputs such as disintegrants, glidants and diluents.
A number of leading pharmaceutical companies have major investments in fine chemical manufacturing, providing
them with a degree of self-sufficiency and this reduces supplier power to an extent. APIs are supplied on a contractual
basis and so pharmaceutical companies are likely to risk high switching costs if they consider taking their business
elsewhere. In turn, pharmaceutical companies employ sourcing managers to minimize costs and to mitigate supplier
power. The development of new therapeutic agents requires the sourcing of newer APIs, for which chemical
manufacturers can charge pharmaceutical companies higher prices. If the novel drug successfully reaches the market,
the supplier of the API can make a large amount of money.
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 customers utilizing a high degree of choice in order 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. Over recent years, larger
pharmaceutical companies have turned to producing their own chemicals in a bid to enhance profits; however,
smaller companies lack the resources required to do this and remain reliant on API manufacturers.
It is common for pharmaceutical companies to outsource their 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.
Overall, supplier power is moderate.
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Regulation and legal frameworks can affect the ease of market entry in several ways.
Firstly, a company wishing to market its products must demonstrate that its drugs are safe and effective, to the
satisfaction of the national regulator. In India, this role is played by the Drug Standard Control Organization (CDSCO).
Companies must adhere to stringent manufacturing practice and quality control standards with the production of
generics. Historically, this regulation has been more lax than in many other countries, with one 2014 study finding
10% of pharmaceuticals studied to be of poor quality, and a Europe-wide ban on generics from Indian company GVK
Biosciences coming into effect in mid-2015.
A start-up company that intends to develop an entirely new biotech drug will need significant up-front investment,
often from venture capital companies, and this must be available for the time it takes to develop and test the product.
Meeting these regulatory requirements is time-consuming; it can take 10 to 15 years to bring a drug to market.
According to the Pharmaceutical Research and Manufacturers of America (PhRMA), out of 5,000 to 10,000 screened
compounds, only 250 enter preclinical testing, of which only five enter human clinical trials, and finally just one will be
approved. In addition to investing a significant amount in research and development, manufacturers also expend
substantial costs on marketing, which further increases the capital required by new entrants.
On the other hand, entering a specific country market with an existing drug is likely to be easier, provided the
licensing authority there is satisfied.
A further regulatory barrier to entry is the use of restrictive formularies: for a specific therapeutic category, only
certain drugs may be listed as preferred. This does not mean that non-formulary alternatives are unsafe or ineffective.
Rather, they can only be prescribed in special circumstances with prior approval from the relevant authority, or with
more substantial co-pays from the patient. The potential market for non-formulary drugs will therefore be smaller
than the size of the therapeutic class market might imply.
Due to the relatively low manufacturing costs of small molecules, patent protection is the major barrier to entry for
new entrants into the market. The intensity of competition can result in significant legal action around the time a
major drug reaches the end of its patent life, particularly for ‘blockbuster’ drugs that sell more than $1bn a year.
Secondary patents covering new alterations in the drug formulation, dosing regimens, or methods of administration,
are usually pursued, prompting litigation between major pharmaceutical and generics companies. Indeed, it is usually
worthwhile for a manufacturer to spend millions in legal fees in order to delay the launch of a new generic product by
a number of weeks, due to the profitability of major blockbuster drugs.
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The nature and strength of intellectual property protection is dependent on the specific market; however, compliance
with international IP legislation is improving in the developing markets, particularly where these markets are shifting
to knowledge-led economies.
New entrants will also have to recruit specialists in the field, in order to develop and produce innovative medications.
Researchers often have a bachelor’s degree in chemistry or a related field, potential employees with qualifications of
this nature often command higher salaries, which could prove to be a barrier for new entrants.
Increased regulatory scrutiny from authorities and consolidation in the supply chain to the US has resulted in greater
research and development expenses, along with other price pressures. Several existing players are now targeting
specialty drugs and complex therapies, showing the Indian market is undergoing significant development in terms of
sophistication. Increasing prosperity among the general population and greater demand for improving healthcare will
attract new entrants seeking new markets. For foreign companies, increasingly stringent controls, which are closer to
standards common in more developed markets, could make India a more enticing prospect because the risk of brand
damaging scandals is reduced. The number of drug approvals in the US for drugs made in India increases
attractiveness to new entrants.
Current market players, with whom new entrants must compete, are well-established companies who benefit from
scale economies. These include leading generic companies such as SunPharma and Lupin, as well as domestic
company Aurobindo. 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. Also, laws defending intellectual property vary from country to
country. In some, patent law may be undeveloped. In others, governments may explicitly prioritize public health
needs over private intellectual property rights. India did not allow drugs to be patented until 2005 (in line with WTO
requirements), and currently only grants patents to completely new drugs rather than improvements to existing
products.
Overall, whilst the barriers to market entry are relatively high, strong market growth means that the threat of new
entrants is weak.
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There are several substitutes for pharmaceuticals considered in this report. Patients may choose traditional remedies.
Physicians may opt for non-drug treatments if they consider them more appropriate. Successful drugs coming off
patent also allow buyers to purchase generic drugs.
Switching costs for patients here are relatively low. However, they may be more significant for the ultimate buyers,
the healthcare providers. For example, suppose a national healthcare system reviewed the clinical evidence and
decided that a chronic condition that had been treated by drugs taken for the patient’s lifetime could actually be
treated by a simple surgical procedure. This would be a beneficial and cheap alternative. However, it might require
more surgical teams to be trained and more operating theatres made available, which the healthcare system would
also need to fund. These would constitute switching costs.
The main substitutes to branded drugs are generics and biosimilars (also known as follow-on biologics).
Manufacturers of generics can offer the same drug at a much lower price, as they rely on the safety and efficacy data
provided by the innovator product, and they therefore do not have to conduct costly clinical trials.
In April 2017, the Indian Supreme Court upheld a ruling which stated that Swiss pharmaceutical company Novartis
should not receive a patent for its leukemia drug Gleevec. Many hope the ruling will prevent pharmaceutical
companies from seeking patents on HIV drugs and other medicines. However, some observers fear any further free
trade agreements could unwind progress made towards greater protection for generic drugs.
The threat of substitutes is assessed as strong.
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The Indian research-based pharmaceuticals market is dominated by several large corporations, alongside smaller firms
such as biotech players focused on a small number of new products; generics companies are also present. The
presence of large incumbents, as well as the number of companies operating within the market, increases the level of
rivalry. The leading players in the market include Aurobindo, Lupin, Dr Reddys Labs and Sun Pharmaceutical Industries
Limited.
Rivalry in the Indian market is alleviated somewhat by the strong rate of growth and importance as an exporting
nation of pharmaceuticals. Aurobindo Pharma was recently granted final approval from the US health regulator to
manufacture abacavir sulfate and lamivudine tablets, used in the treatment of HIV. Success as an export nation and
growing consumption of healthcare services has produced a growing market in which companies can expand without
resorting to mergers and acquisitions. Aurobindo, a leading company in India, has produced rapid growth in profits
and revenues during recent years. However, the market is fragmented compared to more developed countries and
consolidation will serve to increase rivalry.
Large companies often lose revenue due to the expiration of patents and are increasingly motivated to acquire
smaller companies that have a strong revenue potential due to innovative products. Therefore, acquisitions are
common in this particular market and are a key way for companies to establish a competitive edge.
The practical benefit is reducing overall costs by increasing specialization, therefore eliminating research in less
profitable areas. The downside is the possibility that drugs will be produced by fewer companies, decreasing the
chance of major breakthroughs.
However, market concentration overall is not very high. There may be a greater effective concentration within specific
therapy areas, and this is a market where products can be highly differentiated through their clinical effectiveness. For
example, one company may have a patented drug which is highly effective in treating a particular condition. It would
be difficult to compete directly with such a player, although other companies will no doubt be managing development
pipelines in order to exploit this market when the drug comes off patent.
Research-based pharmaceutical companies are similar to media companies, in that they rely on initially creating
valuable intellectual property at a high cost, which can then be used to create mass-produced products at relatively
low cost. 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 research-based companies to expand
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output, for example through licensing agreements with other companies, without the need to scale up their own
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 market. Many of the assets are ‘weightless’ – patents, trademarks, synthetic methods,
and so on – and can be sold relatively easily. Many of the R&D and production facilities and equipment have uses
outside pharmaceutical research or manufacture.
Overall, the degree of rivalry is strong.
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7. Competitive Landscape
The Indian pharmaceutical market is dominated by several multinational corporations, alongside smaller firms, such as
biotech players, which are focused on a small number of new products. The presence of large international
incumbents, and the large number of companies operating within the market, has intensified competition in the
market. The Indian market is highly fragmented, with the four leading players accounting for just 8.3% of the market’s
total value.
Company % Share
Lupin 3.5%
Sun Pharmaceutical Industries Limited 3.5%
Dr Reddys Labs 0.9%
Aurobindo 0.4%
Other 91.7%
Total 100%
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Lupin Ltd (Lupin) develops and manufactures generic and branded formulations, biotechnology products and active
pharmaceutical ingredients (APIs). It is one of the leading players in India, with a market share of 3.5%. The company
has expertise in the areas of cardiovascular, asthma, diabetology, pediatrics, central nervous system, gastro-intestinal,
anti-infectives, nonsteroidal anti-inflammatory drugs (NSAIDs), anti-TB and cephalosporins.
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. It also has a market share of
3.5%. The company’s products find application in the treatment of various conditions related to psychiatry, neurology,
cardiology, nephrology, gastroenterology, orthopedics and ophthalmology.
Dr. Reddy's Laboratories (DRL) is an integrated pharmaceutical company that offers generics, over the counter, active
pharmaceutical ingredients and proprietary products. The generics products are ready for consumption by the
customer product and specified for the areas of gastrointestinal, cardiovascular, pain management, oncology, anti-
infectives, pediatrics and central nervous system. DRL has a market share of 0.9%.
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 (CNS), cardiovascular, anti-allergies, anti-diabetics, other therapeutic areas. It is the smallest of the four
leading players, with a market share of 0.4%.
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INR15,730.9 million ($2.2 billion), which as a percentage of revenue amounted to 9.4%. Lupin operates research
facilities in the Netherlands, Mexico, Brazil; Japan; and in the US.
7.5. What has been the rationale behind recent M&A activity?
Sun Pharma has implemented strategic inorganic initiatives, which will enhance its business operations in the long
term. The company acquired an additional 11.86% stake in Biosintez in March 2019. With this additional stake, Sun
Pharma increased its stake in Biosintez to 96.9%. Biosintez manufactures and markets pharmaceuticals including,
injections, blood preservatives, ampoules, blood substitutes, ointment, creams, tablets, suppositories, gels, and APIs
among others, for hospital segment. Biosintez recorded revenue of RUB2,373 million in 2018. Sun Pharma believes
that the acquisition will enhance its market share in Russia and improve its profitability. The company acquired Pola
Pharma in January 2019. The acquisition is likely to reinforce Sun Pharma’s presence in dermatology segment across
the world. Pola Pharma conducts R&D, manufacture, distribution, and sale of generics and branded pharmaceuticals
in Japan. It operates two manufacturing facilities in Saitama with capabilities to produce topical injectables and
products.
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8. Company Profiles
Lupin Ltd (Lupin) develops and manufactures generic and branded formulations, biotechnology products and active
pharmaceutical ingredients (APIs). The company has expertise in the areas of cardiovascular, asthma, diabetology,
pediatrics, central nervous system, gastro-intestinal, anti-infectives, nonsteroidal anti-inflammatory drugs (NSAIDs),
anti-TB and cephalosporins. It undertakes extensive research and development of pharmaceuticals for treatment of
migraine, gastrointestinal, psoriasis, central nervous system, cardiovascular, tuberculosis, diabetes and inflammation.
Lupin develops value-added generic pharmaceuticals based on its platform technologies. The company along with its
subsidiaries has manufacturing facilities in India, the US, Japan, Mexico and Brazil. Lupin is headquartered in Mumbai,
Maharashtra, India.
The company reported revenues of (Rupee) INR167,181.8 million for the fiscal year ended March 2019 (FY2019), an
increase of 5.8% over FY2018. In FY2019, the company’s operating margin was 8.8%, compared to an operating
margin of 3.8% in FY2018. In FY2019, the company recorded a net margin of 3.6%, compared to a net margin of 1.6%
in FY2018. The company reported revenues of INR44,183.8 million for the first quarter ended June 2019, an increase
of 0.3% over the previous quarter.
Head office: B/4 Laxmi Towers Bandra Kurla Complex, Bandra East, Mumbai, Maharashtra, India
Number of Employees: 17042
Website: www.lupin.com
Financial year-end: March
Ticker: LUPIN
Stock exchange: National Stock Exchange of India
Lupin Ltd (Lupin) undertakes the manufacture and marketing of generic and branded pharmaceutical products, and
active pharmaceutical ingredients (APIs). The company offers these drugs in various formulations such as solid, semi-
solid and liquid. It is one of the leading and fasting growing companies. Its product portfolio is focused on various
therapeutic areas such as cardiovascular, diabetics, asthma, pediatrics, central nervous system, gastro intestinal,
tuberculosis, infections and non-steroidal anti inflammatory drugs.
The company’s operations are limited to one segment, namely, Pharmaceuticals.
Lupin’s business includes formulations, active pharmaceutical ingredients (APIs), generic formulations, and
biotechnology products. The company’s global formulations business develops and delivers a broad range of branded
and generic formulations, biotechnology products and APIs worldwide. Lupin specializes in the diabetology,
cardiovascular, pediatric, asthma, gastrointestinal, central nervous system (CNS) therapeutics, anti-infectives, anti-TB
and nonsteroidal anti-inflammatory drugs (NSAID) space. Principal markets of formulations business include India, the
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US, Japan, Europe, South Africa, Philippines, and Australia. The business operates 18 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 biosmilars. It has
a pipeline of ten biosimilars in various stages of clinical development.
Lupin commercialized oncology products: Lupifil and Lupifil-P, biosimilars for molecules Filgrastim and Peg-Filgrastim
in India four years ago. 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, Japan, the US, Brazil and Mexico. It sells its products to over
100 countries in the US, the UK, Europe, Germany, India, Japan, South Africa, Philippines, and Australia through a
network of international subsidiaries and a Joint Venture in Japan.
Geographically, the company generates its revenue from four regions, namely, India, the US, Japan and other.
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Sun Pharmaceutical Industries Inc (Sun Pharma), a subsidiary of Sun Pharmaceutical Industries Ltd, is a healthcare
products provider that manufactures pharmaceuticals products. The company offers generics, branded generics, over
the counter (OTC), and prescription products. Its generic products include allopurinol, albuterol USP, bromocriptine
mesylate USP, calcitriol, clopidogrel USP, desloratadine, doxycycline hyclate, fenofibrate, imatinab, valsartan,
zonisamide, and others. Sun Pharma’s OTC products comprise cholesterol control, vitamins and minerals supplement,
olesan oil, and nasal decongestant. The company serves therapeutic areas of neurology, cardiology, anti-infectives,
ophthalmology, gynaecology, respiratory, oncology, nephrology, diabetology, gastroenterology, and nutritionals. It
operates in Israel and Hungary. Sun Pharma is headquartered in Cranbury, New Jersey, the US.
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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 (CNS), cardiovascular, anti-allergies, anti-diabetics, other therapeutic areas. The company also produces novel
proprietary biocatalysts, dietary supplements and fermentation based semi synthetic products. Aurobindo operates
manufacturing facilities in India, the US, Brazil and Portugal; 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) INR195,635.5 million for the fiscal year ended March 2019 (FY2019), an
increase of 18.6% over FY2018. In FY2019, the company’s operating margin was 16.4%, compared to an operating
margin of 19.7% in FY2018. In FY2019, the company recorded a net margin of 12.1%, compared to a net margin of
14.7% in FY2018. The company reported revenues of INR54,446 million for the first quarter ended June 2019, an
increase of 2.9% over the previous quarter.
Plot No. 11 Survey No. 9, Water Mark Building, Kondapur, Hitech City, Hyderabad,
Head office:
Telangana, India
Number of Employees: 17332
Website: www.aurobindo.com
Financial year-end: March
Ticker: AUROPHARMA
Stock exchange: National Stock Exchange of India
Aurobindo Pharma Ltd (Aurobindo) is a global pharmaceutical company that produces generic formulations and active
pharmaceutical ingredients (APIs). The company’s product portfolio is spread over seven key therapeutic areas,
including antibiotics, antiretrovirals (ARVs), cardiovascular, central nervous systems (CNS), anti-diabetics,
gastroenterologicals and antiallergics. It offers a broad portfolio of diversified dosage forms, including prescription
and OTC oral solids and liquids, specialty products ophthalmics, injectables and controlled substances.
Aurobindo manufactures and sells generic formulations in the US, Europe and growth markets. It principally develops
oral and injectable generic formulations. The company also provides customer centric project-based chemistry
services and stability study activities through AuroSource; novel slutions 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.
- Markets products and solutions in more than 150 countries.
- Manufactured more than 26 billion diverse dosage forms in FY2018
- It has several manufacturing facilities for APIs-oral and sterile, drug intermediates and formulations. Operates 21
manufacturing facilities in India, three manufacturing facilities in the US and one each in Brazil and Portugal; and R&D
facilities in India and USA
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Dr. Reddy's Laboratories (DRL or 'the company') is an integrated pharmaceutical company that offers generics, over
the counter, active pharmaceutical ingredients and proprietary products. The generics products are ready for
consumption by the customer product and specified for the areas of gastrointestinal, cardiovascular, pain
management, oncology, anti-infectives, pediatrics and central nervous system. It also offers pharmaceutical services
and active ingredients product that consists of active pharmaceutical products or bulk drugs. DRL is engaged in the
discovery of new chemical entities for the areas of metabolic disorders, pain and inflammation. The company
operates in India, North America, Europe, Russia and other countries of the former Soviet Union. DRL is
headquartered in Hyderabad,Telengana, India.
The company reported revenues of (Rupee) INR154,482 million for the fiscal year ended March 2019 (FY2019), an
increase of 8.2% over FY2018. In FY2019, the company’s operating margin was 13.2%, compared to an operating
margin of 8.9% in FY2018. In FY2019, the company recorded a net margin of 12.6%, compared to a net margin of 6.6%
in FY2018. The company reported revenues of INR38,582 million for the first quarter ended June 2019, a decrease of
4.3% over the previous quarter.
Dr. Reddy's Laboratories (DRL or 'the company') is a pharmaceutical company engaged in manufacturing generics,
active pharmaceutical ingredients (APIs), and proprietary products. It primarily operates in India, North America,
Europe, Russia and other countries of the former Soviet Union.
The company operates through four segments: global generics; pharmaceutical services and active ingredients (PSAI);
proprietary products; and other.
DRL's global generics segment consists of finished pharmaceutical products that are ready for consumption by the
patient. These products are marketed under a brand name (branded formulations) or as generic finished dosages with
therapeutic equivalence to branded formulations (generics).The branded generics portfolio offers products in the
therapeutic areas of gastrointestinal, cardiovascular, pain management, oncology, anti-infectives, pediatrics and
central nervous system under the brand names of Omez, Ciprolet, Nise, Ketorol, Stamlo, Razo and Cetrine in India,
Russia, Venezuela, Romania, South Africa and certain countries of the former Soviet Union. The segment is also
engaged in over-the-counter (OTC) drug products business. DRL's biologics business is also a part of the company's
global generics segment. In FY2019, the global generics segment reported the revenue of INR122,903 million, which
accounted for 79.9% of company’s total revenue.
The PSAI segment consists of the company's APIs and intermediates, also known as active pharmaceutical products or
bulk drugs, which are the principal ingredients for finished pharmaceutical products. This segment also manufactures
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and sells APIs and steroids in accordance with the specific customer requirements. In addition, the PSAI segment
offers contract research services. In FY2019, the PSAI segment reported the revenue of INR24,140 million, which
accounted for 15.7% of company’s total revenue.
The company's proprietary products is engaged in the discovery of new chemical entities (NCEs) and differentiated
formulations for subsequent commercialization and out-licensing. It also includes the company's specialty
pharmaceuticals business which sells and markets in-licensed and co-developed dermatology products. The NCE's
therapeutic areas of focus include metabolic disorders, pain and inflammation. In FY2019, the proprietary products
segment reported the revenue of INR4,750 million, which accounted for 3.1% of company’s total revenue.
The Other segment includes the operations of company’s wholly-owned subsidiary, Aurigene Discovery Technologies
Limited. The subsidiary is a discovery stage biotechnology company that develops therapies for oncology and
inflammation and works with established pharmaceutical and biotechnology companies. In FY2019, the other
segment reported the revenue of INR2,058 million, which accounted for 1.3% of company’s total revenue.
Geographically, the company classifies its operation into four countries including the US, India, Russia and Others. In
FY2019, the company generated 45% of revenue from the US, followed by India (18.7%), Russia (9.9%) and other
(26.3%).
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9. Macroeconomic Indicators
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Appendix
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provide the foundation for all related industry profiles
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MarketLine aggregates and analyzes a number of secondary information sources, including:
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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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Peninsula Chambers, Ground Floor, Ganpatrao Kadam Marq, Lower Parcel, Mumbai 400 013, IND
Tel.: 91 22 249 18123
Fax: 91 22 249 15168
www.indiaoppi.com
Generics in Europe
Global Pharmaceuticals
Pharmaceuticals in the United States
Pharmaceuticals in Asia-Pacific
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