The document is a regulatory filing containing the transcript of the Q2 FY27 post-results earnings call held on November 4, 2026, submitted pursuant to SEBI Listing Regulations 30 and 46(2)(oa).
The event was an earnings call to discuss the financial and operational performance for the quarter ended September 30, 2026 (Q2 FY27).
The call was held on November 4, 2026. A specific time was not mentioned in the transcript.
The stated purpose was to discuss the company's quarterly results and provide a strategic update.
The meeting was held after the earnings announcement, as it is explicitly a "post-results" call.
Management participants included:
Dr. Sharvil Patel - Managing Director
Mr. Ganesh Nayak - Director
Mr. Tushar Shroff – Chief Financial Officer
Mr. Arvind Bothra - Head, Investor Relations
Mr. Alok Garg - MD Office
The transcript itself was made available as an attachment to this regulatory filing. There was no mention of a presentation deck, recording, or a specific hosting location for those materials.
The transcript contained extensive financial data and operational highlights from the concluded quarter.
Financial Highlights from Transcript
Consolidated Revenue: ₹79.1 billion, up 29% Year-on-Year (YoY).
EBITDA Margin: 24%.
Reported EBITDA: ₹18.9 billion.
Adjusted EBITDA Margin: 25.5% (when adjusted for Saroglitazar launch investments).
Net Profit: ₹9.3 billion.
Net Debt to EBITDA: 0.62x as of September 30, 2026.
R&D Spend: Approximately ₹6.5 billion for the quarter.
Business Segment Performance
India Branded Formulations: Revenue grew 19% YoY. Secondary sales grew 20% YoY, with volume and new products contributing ~2/3 of growth. Chronic portfolio contribution stood at 56.9%.
International Formulations (ex-North America): Revenue of ₹10 billion, up 33% YoY.
North America (US & Canada): Revenue of ₹33.1 billion, up 21% YoY and 7% Quarter-on-Quarter (QoQ). Specialty products accounted for 16% of US revenue.
Consumer Wellness: Revenue of ₹11.2 billion, up 76% YoY. Domestic business grew 29% YoY.
Medical Devices: Revenue of ₹2.2 billion for the quarter.
Strategic Updates & Guidance
USFDA Inspections: The SEZ-II, Ahmedabad facility received 1 observation; the Moraiya facility received 5 observations. The company is addressing them.
US Launch Pipeline: Filed 4 ANDAs, received 12 approvals, and launched 5 products in Q2, including the first generic of Riociguat in October 2026.
Saroglitazar (US): Expecting a potential approval (goal date in November 2026) and planning for a commercial launch in March 2027. Annual commercial spend is estimated at ~$100 million. Meaningful revenue is expected from FY30.
Biosimilars: USFDA accepted the BLA for a Pembrolizumab (Keytruda) biosimilar for review.
Acquisitions: Rolvedon (from Assertio) is contributing to US specialty growth.
Outlook: The company maintains its FY27 guidance of 24%+ EBITDA margin. For the US business, it guides for high single-digit growth on a constant currency basis for FY27.
Additional Notes Section
The regulatory filing had one attachment: the full transcript of the earnings call.
Significant financial data and forward-looking statements were disclosed within the attached transcript.