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10 of 86 filings·Updated 24 Aug 2026
Showing 10 of 86 filings.
24 Aug 20261 filing
Company UpdateGeneral

Lupin receives independent ESG rating of 60 (Adequate) based on public data

ESG Rating Disclosure

  • ESG rating of 60 assigned to Lupin, category Adequate, by ESG Risk Assessments & Insights Limited.
  • Lupin did not engage the firm; rating prepared from Lupin's public-domain data.
  • Disclosure for information and dissemination.
Filed 18:53View Source
20 Aug 20261 filing
Company UpdateGeneral

Lupin subsidiary signs exclusive YUVEZZI license in Europe with Visus Therapeutics; up to €75m in milestones

Exclusive license for YUVEZZI in Europe

  • Exclusive license to commercialize YUVEZZI in EU, UK, Switzerland, Norway, Iceland.
  • Parties: Lupin's VISUfarma B.V. and Visus Therapeutics, Inc. (Tenpoint subsidiary).
  • Initial term 20 years from first commercial sale per country; renewals possible in five-year steps.
  • Total potential consideration up to €75 million (up to €20m SAFE investment; up to €55m milestones).
  • Milestones include regulatory and commercial payments; royalties based on net sales.
  • Not a related-party transaction; no promoter interest in the arrangement.
  • Strategic expansion strengthens Lupin's ophthalmology portfolio in Europe and growth opportunities.
Filed 10:54View Source
18 Aug 20261 filing
Company UpdateDemise

Lupin reports demise of Dr. Sofia Mumtaz, President, Legal & Compliance, Aug 17, 2026

Demise of Senior Management Personnel

  • Dr. Sofia Mumtaz, President, Legal & Compliance for Canada, ANZ & NEA, died on August 17, 2026.
  • Cessation of her Senior Management Personnel role due to demise.
Filed 22:10View Source
17 Aug 20262 filings
Company UpdatePress Release / Media Release

Lupin secures US FDA final approval for Pitolisant Tablets (4.45 mg and 17.8 mg)

FDA approval

  • US FDA grants final approval for Pitolisant Tablets, 4.45 mg and 17.8 mg.
  • Bioequivalent to Wakix® for indications in the approved labeling.
Filed 12:21View Source
Company UpdatePress Release / Media Release

Lupin receives US FDA final approval for Pitolisant tablets, bioequivalent to Wakix

Regulatory approval

  • FDA grants final approval for Pitolisant tablets, 4.45 mg and 17.8 mg.
  • Approved as bioequivalent to Wakix® per the approved labeling.
  • Approval obtained via Lupin's Abbreviated New Drug Application (ANDA).
Filed 12:19View Source
12 Aug 20261 filing
Company UpdateEarnings Call Transcript

Lupin posts record Q1 FY2027 revenue and EBITDA; US growth solid, full-year EBITDA guidance around 25%.

Financial Performance

  • Q1 FY27 revenue from operations: INR 8,277 crores; EBITDA ex-forex/other income: INR 2,464 crores.
  • Revenue grew 32% YoY; EBITDA grew 50% YoY; 16th consecutive YoY growth.
  • Gross margin at 74.6% in Q1; up 330 bps vs Q1 FY26.
  • EBITDA margin was 30% in Q1; full-year target around 25%.
  • R&D spend 7.4% of sales; INR 608 crores.
  • Other operating income: INR 60 crores; down 43% YoY due to lower export benefits.
  • Operating working capital: INR 8,260 crores; 90 days of net working capital.
  • Net cash: INR 2,831 crores as of 30 June 2026; 4,636 crores as of 31 March 2026.
  • ROCE: 29.5%; FY26 was 28.4%.
  • ESG progress: 41% GHG reduction, 45% water recycling; TIME sustainability list recognition.

Geography & Segments

  • U.S. sales: USD 366 million in Q1; CC growth 30% YoY.
  • FY27 U.S. revenue target: USD 1.1–1.2 billion.
  • India sales: INR 2,380 crores; 13.9% YoY; core prescription growth 15.1%.
  • Volume growth in India: 6.1%; chronic share ~67% of portfolio.
  • Other Developed Markets: INR 1,149 crores; 14% of sales; YoY +48%; Europe +83%.
  • Emerging Markets: INR 990 crores; YoY +52%; Brazil +117% local currency.

Pipeline & Product Launches

  • Pegfilgrastim launch expected in H2 FY27; 505(b)(2) Dalbavancin in pipeline.
  • Nasal Fluticasone spray; Epinephrine nasal spray; Raltegravir; Eribulin; Diazepam nasal spray in FY27.
  • FY28: Apixaban 505(b)(2); Diazepam nasal; Epinephrine nasal; iron sucrose; Saxenda; Ivacaftor FTF.
  • FY29: Spiriva Respimat filing; Etanercept; potential P4-related timing.
  • Xywav is a FY33 product; MDI capacity is fungible across products.

Guidance & Outlook

  • Near-term US headwinds from Tolvaptan and Mirabegron; growth moderates.
  • FY27 US revenue guidance anchored at USD 1.1–1.2 billion.
  • Full-year EBITDA margins expected around 25%.
  • R&D spend 7.4% of sales; ETR expected 27–28%.
  • US growth to resume from FY28; 50+ US products in pipeline.

Risks & Watchpoints

  • US competition in Tolvaptan and Mirabegron could pressure margins.
  • Geopolitical headwinds and FX volatility remain risk factors.
  • Export benefits under PLI schemes declined; impact on Other Operating Income.
  • FDA EIRs received for Ankleshwar and Somerset; Pithampur remediation ongoing.
Filed 17:43View Source
10 Aug 20262 filings
Company UpdatePress Release / Media Release

Lupin Receives US FDA Approval for Sodium Zirconium Cyclosilicate Oral Suspension Bioequivalent to Lokelma

Regulatory approval

  • US FDA approves Lupin's Sodium Zirconium Cyclosilicate for Oral Suspension, 5 g and 10 g packets.
  • Bioequivalent to Lokelma® for oral suspension; indicated for treatment of hyperkalemia in adults.
  • Lokelma® (RLD) had estimated US annual sales of USD 568 million (IQVIA MAT Jun 2026).
Filed 18:02View Source
Company UpdateAnalyst / Investor Meet

Lupin to participate in five in-person analyst/investor meets in Aug-Sep 2026

Meetings

  • Aug 13, 2026 – Equirus Annual India Conference, in-person group meet; times not disclosed; purpose: analyst/institutional investor discussions.
  • Aug 14, 2026 – Emkay Confluence 2026 – India: Full Throttle Ahead, in-person group meet; purpose: analyst/institutional discussions.
  • Aug 18, 2026 – Motilal Oswal 22nd Annual Global Investor Conference, in-person group meet; purpose: analyst/institutional discussions.
  • Aug 25, 2026 – Antique Healthcare Investor Conference, in-person group meet; purpose: analyst/institutional discussions.
  • Sept 1, 2026 – Ashwamedh Elara India Dialogue 2026, in-person group meet; purpose: analyst/institutional discussions.
  • Presentations at events will follow Lupin’s existing material on company/stock exchange websites.
Filed 16:19View Source
8 Aug 20262 filings
Company UpdateNewspaper Publication

Copies of Newspaper publication in respect of Unaudited Financial Results of the Company for the quarter ended June 30, 2026.

Filed 12:21View Source
Company UpdateCopy of Newspaper Publication

Lupin Limited has informed the Exchange regarding copies of Newspaper Publication regarding Unaudited Financial Results of the Company for the quarter ended June 30, 2026.

Filed 12:15View Source
Showing 10 of 86 filings