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Dr. Reddy's Q4 FY26 revenue (ex-SSA) was INR 7,969 crore, down 6% YoY, dragged by a INR 453 crore lenalidomide shelf-stock adjustment. EBITDA margin of 19.5% (adjusted) missed the 25% aspirational target, impacted by lower gross margins (48%) and higher SG&A. The base business (ex-lenalidomide) grew double-digits. Management expects FY27 gross margins above 50% and EBITDA margins near 25% as semaglutide launches ramp up. Key risks include delayed semaglutide approvals (Brazil) and competitive pricing erosion in U.S. generics.
डॉ. रेड्डी की चौथी तिमाही की कमाई (SSA को छोड़कर) 7,969 करोड़ रुपये रही, जो पिछले साल से 6% कम है। इसकी वजह लेनालिडोमाइड दवा के स्टॉक में 453 करोड़ रुपये का अस्थायी समायोजन था। कंपनी का मुनाफा मार्जिन (EBITDA) 19.5% रहा, जो 25% के लक्ष्य से कम है। इसकी वजह कम सकल मुनाफा (48%) और ज्यादा खर्चे हैं। लेनालिडोमाइड को छोड़कर बाकी कारोबार में दो अंकों की बढ़त हुई। प्रबंधन को उम्मीद है कि अगले साल सकल मुनाफा 50% से ऊपर और EBITDA मार्जिन 25% के करीब होगा, जब सेमाग्लूटाइड जैसी नई दवाएं लॉन्च होंगी। मुख्य जोखिम हैं ब्राजील में देरी और अमेरिका में सस्ती दवाओं की प्रतिस्पर्धा।
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View Promises →Semaglutide approval delays in Brazil
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Read Transcript →Management expects 6-7 million semaglutide units sold by end of calendar 2026 across approved markets.
India revenues grew 20% YoY to INR 1,566 crore, outperforming IPM growth of 11.6%.
North America generics revenue declined 40% YoY due to lower lenalidomide sales and shelf-stock adjustment.
Emerging markets revenue grew 29% YoY to INR 1,806 crore, led by new launches and volume growth.
Management expects gross margins to improve above 50% in FY27, driven by semaglutide launches and cost improvement programs.
EBITDA margin is expected to approach 25% in FY27, aided by semaglutide sales, though may be slightly below.
R&D expenditure is expected to be in the range of 7%-8% of adjusted revenue in FY27.
Capital expenditure for FY27 is guided at approximately INR 2,000 crore, primarily for biosimilars and product-specific investments.
Dr. Reddy's will launch generic Ozempic (diabetes) in India on March 21, with all strengths including oral Rybelsus.
Health Canada response expected between end-February and May 2026, with launch preparation underway for Q4 or Q1.
IV presentation BLA filed December 2025; approval expected around end-2026, with sub-Q filing in July 2026 and launch by Jan/Feb 2028.
From Q4 FY26 onwards, without lenalidomide, global generics and PSAI gross margin expected in 50%-55% range.
Brazil approval for semaglutide is delayed by 3-4 months, which could impact FY27 unit sales guidance of 12 million units.
A surprise INR 453 crore shelf-stock adjustment hit Q4 revenue; similar customer-driven adjustments could recur.
U.S. generics revenue has been flat despite new launches, indicating significant price erosion that may continue.
Impairment of INR 135 crore on CAR T and INR 93 crore on partnered asset (Immutep) highlights R&D pipeline risk.
Denosumab received CRL from FDA due to partner Alvotech's facility issues; Rituximab requires re-inspection. Both face delays of at least 6-12 months.
CEO advised to assume zero lenalidomide revenue from Q4 FY26, which will impact overall revenue and margins.
Management expects eventual competition in Canada and other markets, with pricing likely settling at lower end of $20-$70 range.
SG&A as % of revenue remains elevated at 30% (ex-one-off); management expects growth to moderate but absolute level may not decline.
Mentioned in Q1 FY26, Q3 FY25, Q3 FY26, Q4 FY25
Dr. Reddy's will launch generic Ozempic (diabetes) in India on March 21, with all strengths including oral Rybelsus.
Mentioned in Q1 FY25, Q1 FY26, Q2 FY25, Q3 FY25
R&D investments expected in this range for the full fiscal year.
Mentioned in Q2 FY25, Q2 FY26, Q4 FY25
Revlimid sales are declining faster than expected, with Q3 likely the last quarter of meaningful contribution.
Mentioned in Q2 FY26, Q3 FY25
BLA for abatacept IV will be submitted by end of calendar 2025, with high confidence in approval.
Mentioned in Q1 FY26, Q3 FY25
Lenalidomide sales expected to drop significantly after Q2 FY26; magnitude depends on pricing and competitor behavior.
Management expects gross margins to improve above 50% in FY27, driven by semaglutide launches and cost improvement programs.
Brazil approval for semaglutide is delayed by 3-4 months, which could impact FY27 unit sales guidance of 12 million units.
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