Key Quantitative Figures
Consolidated Results (IFRS):
Q2FY27:
- Revenues: ₹86,708 million (Down 1.5% YoY; Up 7.4% QoQ)
- Gross Margin: 52.1% (Q2FY26: 54.7%; Q1FY27: 46.5%)
- EBITDA: ₹17,828 million (20.6% of revenues)
- Profit Before Tax: ₹12,277 million (14.2% of revenues)
- Profit After Tax (attributable to equity holders): ₹9,250 million (10.7% of revenues)
- Diluted EPS: ₹11.10
H1FY27:
- Revenues: ₹167,413 million (Down 3.5% YoY)
- Gross Margin: 49.4% (H1FY26: 55.8%)
- EBITDA: ₹27,915 million (16.7% of revenues)
- Profit Before Tax: ₹17,803 million (10.6% of revenues)
- Profit After Tax (attributable to equity holders): ₹13,685 million (8.2% of revenues)
- Diluted EPS: ₹16.42
Segment-wise Revenue (Q2FY27):
- Global Generics: ₹77,927 million (90% of total revenues)
- North America: ₹24,890 million (Down 23% YoY)
- Emerging Markets: ₹20,595 million (Up 24% YoY)
- India: ₹18,508 million (Up 17% YoY)
- Europe: ₹13,935 million (Up 1% YoY)
- PSAI: ₹8,310 million (Down 12% YoY)
- Others: ₹471 million (Up 357% YoY)
Branded businesses (India, Emerging Markets, NRT) accounted for 53% of Q2FY27 revenues.
Balance Sheet Highlights (as of September 30, 2026):
- Cash & Cash Equivalents and Other Investments: ₹86,670 million
- Trade Receivables: ₹101,399 million
- Inventories: ₹81,182 million
- Property, Plant and Equipment: ₹115,097 million
- Goodwill and Other Intangible Assets: ₹117,145 million
- Loans and Borrowings: ₹72,287 million
- Trade Payables: ₹36,082 million
- Equity: ₹389,370 million
Other Financial Metrics:
- Operating Working Capital: ₹146,499 million
- Q2FY27 Capital Expenditure: ₹1,900 million
- Q2FY27 Free Cash Flow: ₹1,705 million
- Net Cash Surplus: ₹25,024 million
- Net Debt to Equity: (0.06)
- Annualized RoCE: 9.5%
Dates of Action
- Board Meeting: October 23, 2026 (3:00 PM to 4:38 PM IST)
- Quarter Ended: September 30, 2026
- Half Year Ended: September 30, 2026
- Earnings Call: October 23, 2026 at 19:30 IST
Parties Involved
- Board of Directors of Dr. Reddy's Laboratories Limited
- Statutory Auditors: Deloitte Haskins & Sells LLP
- Subsidiaries: Multiple entities listed in Appendix A of the report
- Partners: Takeda, Gilead Sciences, GARDP Foundation
- Regulators: USFDA, CDSCO, Thai FDA
Business Highlights
- Partnered with Takeda for India's first CDSCO-approved dengue vaccine QDENGA
- Expanded collaboration with Gilead Sciences for lenacapavir for HIV prevention in 120 countries
- Secured Thai FDA approval for zoliflodacin antibiotic with GARDP Foundation
- USFDA approval for rituximab biosimilar in US
- Launched nivolumab biosimilar in India
- First biosimilar approval in India for abatacept IV
- First-to-market launch of sugammadex injection in US
- Generic semaglutide approved in 10 countries
- CDMO business (Aurigene) generated $100+ million revenues in trailing 12 months
- APSL secured long-term manufacturing agreement with global pharma company
Operational Updates
- Semaglutide API issue: Certain batches found out of specification, appropriate measures being taken
- Received VAI classification from USFDA for Mirfield, UK API facility (September 2025)
- Received Form 483 with three observations at Srikakulam, AP facility (July 2026)
- Received Form 483 with four observations at Bachupally, Hyderabad facility (August 2026)
- Received Form 2953 with two observations at Mexico API facility (July-September 2026)
- Terminated distribution agreement with Novartis India due to change in controlling shareholding
Financial Impact Notes
- Q1FY27 included ₹2,397 million provision for semaglutide API related impact
- Growth impacted by lower lenalidomide revenues in North America
- Underlying base business (ex-lenalidomide) delivered double-digit growth
- FY26 included ₹4,530 million reduction in revenue from lenalidomide price adjustment
- FY26 included various impairment charges including CAR-T program discontinuation
Forward-looking Statements
Management commentary included forward-looking statements about focusing on strengthening core businesses, enhancing productivity, and investing in strategic growth platforms. The document contains customary disclaimer about forward-looking statements being subject to risks and uncertainties.