Cipla (CIPLA) Q2 25/26 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 25/26 earnings summary
6 Jan, 2026Executive summary
Achieved record quarterly revenue of INR 7,589 crore in Q2FY26, up 8% year-over-year, with robust profitability and strong performance across India, U.S., Africa, and EMEU markets.
EBITDA reached INR 1,895 crore (25% of revenue), and PAT was INR 1,351 crore (17.8% of revenue), both showing year-over-year growth.
Maintained leadership in chronic therapies, expanded consumer health, and launched new products in North America and Africa, including entry into obesity care with tirzepatide (Yurpeak) via Eli Lilly partnership.
U.S. business saw $233 million in revenue, with leadership in albuterol MDI and the launch of the first biosimilar (filgrastim).
Unaudited consolidated and standalone financial results for the quarter and half year ended 30th September 2025 were approved and released, with statutory auditors providing an unmodified review conclusion.
Financial highlights
Quarterly revenue grew 8% year-over-year to INR 7,589 crore, the highest ever, with half-year consolidated revenue at INR 14,546.91 crore.
EBITDA margin at 25%; gross margin at 67%; PAT margin at 17.8% of revenue.
Profit after tax was INR 1,351 crore for the quarter and INR 2,644.98 crore for the half year.
R&D investment for the quarter was INR 539 crore (7.1% of revenue), trending higher due to accelerated filings and new programs.
Net cash balance at INR 9,901 crore after debt and dividend payout; cash and cash equivalents increased to INR 10,368 crore year-over-year.
Outlook and guidance
Full-year EBITDA margin guidance revised to 22.75%-24% (from 23.5%-24.5%), excluding Yurpeak business, due to higher R&D spend and lower Revlimid contribution.
India business aims to regain growth momentum and outperform the market in branded and trade generics.
U.S. business expects continued growth in base business, with minimal Revlimid contribution in coming quarters and a sales target of $1 billion next year, contingent on timely approvals.
Pipeline includes four major respiratory launches (including generic Advair) and three peptide assets by 2026.
Management expects a favorable outcome in ongoing litigation with the NPPA and has not made provisions for the related demand notices.
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