Lupin Pharmaceuticals

Lupin Pharmaceuticals

Global pharmaceutical manufacturer and distributor

Overview

Lupin Limited develops and sells branded and generic medicines, complex generics, biotechnology products, and active pharmaceutical ingredients across over 100 markets. It brings medicines to patients by designing formulations and APIs, manufacturing at 15 sites, and distributing through a global network, supported by 7 research centers. Its integrated model combines a broad product portfolio with dedicated manufacturing, diagnostics, digital health, and manufacturing services to serve multiple therapeutic areas. Its goal is to improve patient health outcomes by expanding access to high-quality medicines and strengthening its global research, manufacturing, and digital capabilities.

Significant Headcount Growth

About Lupin Pharmaceuticals

Simplify's Rating
Why Lupin Pharmaceuticals is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Industrial & Manufacturing

Healthcare

Company Size

10,001+

Company Stage

IPO

Headquarters

Mumbai, India

Founded

1968

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Simplify's Take

What believers are saying

  • Q1 FY27 revenue reached INR 82.77 billion on August 7, 2026, beating estimates.
  • FY26 US sales hit $1.3 billion, driven by new launches and mix improvement.
  • Sutab brings 180-day exclusivity and $132.8 million annual-sales upside.

What critics are saying

  • Management guided FY27 EBITDA margin down to 25% from 29.7% on May 9, 2026.
  • Tolvaptan and mirabegron competition already threatens U.S. revenue from Q2 FY27 onward.
  • If U.S. launches slip, Lupin's margin expansion story collapses under generic price erosion.

What makes Lupin Pharmaceuticals unique

  • Lupin won 2026 FDA approvals for Pitolisant, Sugammadex, Sutab, and Ranibizumab.
  • Its first China launch, oseltamivir suspension, entered paediatrics through Yabao in 2026.
  • Nanomi's Philippines stake deepens Lupin's emerging-market control beyond U.S. generics.

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Funding

Total Funding

$50M

Above

Industry Average

Funded Over

1 Rounds

Post IPO Equity funding comparison data is currently unavailable. We're working to provide this information soon!
Post IPO Equity Funding Comparison
Coming Soon

Stock Price

Growth & Insights and Company News

Headcount

6 month growth

15%

1 year growth

15%

2 year growth

15%
PR Newswire
Aug 17th, 2026
Lupin receives US FDA approval for generic Pitolisant tablets

Lupin Limited has received final approval from the US Food and Drug Administration for its generic Pitolisant Tablets in 4.45 mg and 17.8 mg strengths. The FDA approved Lupin's tablets as bioequivalent to Wakix for the indications in the approved labelling. Lupin is a Mumbai-based global pharmaceutical company that distributes products in over 100 markets. The company specialises in branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients. It operates 15 manufacturing sites and six research centres globally, employing over 26,000 professionals.

PR Newswire
Jul 30th, 2026
Lupin launches generic Sugammadex injection in US after FDA approval

Lupin Limited has received US FDA approval and launched Sugammadex Injection in the United States. The product is available in two strengths: 200 mg/2 mL and 500 mg/5 mL single-dose vials. Sugammadex Injection is bioequivalent to Merck's Bridion Injection. It is indicated for reversing neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adults and paediatric patients aged 2 years and older undergoing surgery. Lupin is a Mumbai-based pharmaceutical company with products distributed in over 100 markets. The firm specialises in branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients. It operates 15 manufacturing sites and 7 research centres globally, employing over 26,000 professionals.

Multibagg AI
Jul 2nd, 2026
Lupin subsidiary to acquire 43.38% stake in Philippines' MPPI for up to $39.6M by May 2026

Lupin Ltd announced its subsidiary Nanomi B.V. will acquire a 43.38% stake in Multicare Pharmaceuticals Philippines Inc for up to $39.6 million in cash, with completion expected by end-May 2026. The deal involves purchasing 11,794,497 shares from existing shareholders to strengthen Lupin's presence in the Philippines. Separately, MPPI executed a buyback of 2,813,811 shares using retained earnings. As Nanomi did not participate, its holding automatically increased from 51% to 56.28%. MPPI reported turnover of PHP 2,096.60 million and net worth of PHP 1,265.50 million as of 31 March 2025. Lupin's shares fell 2.52% in early trade on 2 April following the announcement, trading at ₹2,216.20 on BSE.

PR Newswire
Jun 26th, 2026
Lupin receives tentative US FDA approval for generic Enzalutamide tablets

Lupin Limited has received tentative approval from the US FDA for its Enzalutamide Tablets in 40mg, 80mg, 120mg and 160mg strengths. The 40mg and 80mg versions were approved as bioequivalent to Astellas' Xtandi Tablets. Whilst Xtandi traditionally comes in 40mg and 80mg strengths, Lupin's tentatively approved 120mg and 160mg formulations will offer healthcare providers and patients additional dosing options. The Mumbai-based pharmaceutical company distributes products in over 100 markets globally. Lupin operates 15 manufacturing sites and seven research centres worldwide, employing over 24,000 professionals. The company specialises in branded and generic formulations, complex generics, biotechnology products and active pharmaceutical ingredients across multiple therapy areas including respiratory, cardiovascular and anti-diabetic treatments.

PR Newswire
Jun 4th, 2026
Lupin's Ranluspec wins US FDA approval as only interchangeable biosimilar ranibizumab in vials and syringes

Lupin Limited has received US FDA approval for Ranluspec (ranibizumab-hkdz), an interchangeable biosimilar referencing Genentech's Lucentis. Ranluspec is the only interchangeable biosimilar ranibizumab approved in the United States available in both vials and pre-filled syringes. The drug is approved in two strengths, 0.3mg and 0.5mg, for treating neovascular age-related macular degeneration, macular oedema following retinal vein occlusion, diabetic macular oedema, diabetic retinopathy and myopic choroidal neovascularization. Ranibizumab is a recombinant humanised monoclonal antibody fragment that inhibits vascular endothelial growth factor A. This marks Lupin's second US biosimilar approval. The Mumbai-based pharmaceutical company distributes products in over 100 markets globally and employs over 24,000 professionals across 15 manufacturing sites and seven research centres.

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