Glenmark Announces Q3 FY26 Results, India Revenue Up 22.1%

Glenmark Pharmaceuticals reported strong Q3 FY26 results with consolidated revenue at Rs. 39,006 Mn, a 15.1% YoY increase. India formulations revenue grew by 22.1% to Rs. 12,986 Mn. EBITDA stood at Rs. 8,697 Mn, up 44.9% YoY, with a margin of 22.3%. Profit After Tax (PAT) was Rs. 4,032 Mn, a 15.9% YoY rise, with a 10.3% margin.

Financial Highlights for Q3 FY26

Glenmark Pharmaceuticals announced its financial results for the third quarter ending December 31, 2025, showcasing significant growth across various segments:

  • India Formulations: Revenue increased by 22.1% YoY, reaching Rs. 12,986 Mn.
  • North America: Revenue grew by 24.2% YoY to Rs. 9,706 Mn, including out-licensing income.
  • Europe: Revenue rose by 9.1% YoY to Rs. 7,963 Mn.
  • Emerging Markets: Revenue increased by 8.4% YoY to Rs. 8,119 Mn.
  • EBITDA: Achieved Rs. 8,697 Mn, a 44.9% YoY increase, with an EBITDA margin of 22.3%.
  • Profit After Tax (PAT): Reached Rs. 4,032 Mn, a 15.9% YoY increase, with a PAT margin of 10.3%.

Revenue Performance

Consolidated revenue for Q3 FY26 reached Rs. 39,006 Mn, compared to Rs. 33,876 Mn in the corresponding quarter of the previous year, marking a 15.1% YoY growth. For the nine months of FY26, Glenmark’s consolidated revenue was Rs. 132,119 Mn, compared to Rs. 1,00,655 Mn in the previous year, reflecting a 31.3% YoY growth.

Key Strategic Developments

Glenmark has focused on key strategic developments during the quarter, including:

  • Launch of NEBZMART® GFB Smartules® and Glenmark AIRZ® FB Smartules®, the world’s first nebulized, fixed-dose triple therapy for COPD.
  • Partnership with BeOne Medicines for TEVIMBRA® (Tislelizumab) & BRUKINSA® (Zanubrutinib).
  • The company was the first to launch the biosimilar of Liraglutide under the brand name LIRAFIT™ in India.

North America Outlook

North America recorded revenues of Rs. 9,706 Mn for Q3 FY26. The company launched 4 products, and plans to file three ANDAs in the upcoming quarter. Glenmark received the Establishment Inspection Report (EIR) from the U.S. FDA for its manufacturing facility in Monroe.

Global Innovative Portfolio

  • RYALTRIS® marketing applications have been submitted to over 90 countries and is commercialized in 52 markets.
  • WINLEVI® launched in the UK and saw strong uptake.
  • Glenmark filed QiNHAYO™ MA Applications in 18 markets.
  • Advancements for initiation of MA applications for Trastuzumab Rezetecan.
  • Glenmark entered into an agreement for Aumolertinib.

Source: BSE

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