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DRREDDY Diversified 2026-04-??

Dr. Reddy's Laboratories Limited — Q4 FY26

Dr.

neutral medium
Compare with...
Revenue ₹7,546 Cr -6%
EBITDA ₹1,554 Cr -37%
PAT ₹221 Cr
EBITDA Margin 5%
Duration
Read Time 1 min read

✓ Verified against BSE filing

2-Minute Summary

✦ AI-Generated from Full Transcript

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.

Promises0 met · 3 missedRisks4 trackedTranscriptfull text
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Promises 3 promises

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0 delivered, 0 close, 3 missed.

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Risk Intelligence

Semaglutide approval delays in Brazil

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Transcript Full text

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Quarter Snapshot

Semaglutide unit sales guidance (CY 2026) 6-7 million units
N/A

Management expects 6-7 million semaglutide units sold by end of calendar 2026 across approved markets.

India business growth (Q4 YoY) 20%
+20% YoY

India revenues grew 20% YoY to INR 1,566 crore, outperforming IPM growth of 11.6%.

North America generics revenue (ex-SSA) $251 million
-40% YoY

North America generics revenue declined 40% YoY due to lower lenalidomide sales and shelf-stock adjustment.

Emerging markets revenue growth (Q4 YoY) 29%
+29% YoY

Emerging markets revenue grew 29% YoY to INR 1,806 crore, led by new launches and volume growth.

What Changed vs Last Quarter

Comparing Q4 FY26 vs Q3 FY26
4 new guidance4 dropped4 new risk4 risk resolved
NEW
FY27 gross margin above 50%

Management expects gross margins to improve above 50% in FY27, driven by semaglutide launches and cost improvement programs.

NEW
FY27 EBITDA margin near 25% with semaglutide

EBITDA margin is expected to approach 25% in FY27, aided by semaglutide sales, though may be slightly below.

NEW
FY27 R&D spend 7%-8% of revenue

R&D expenditure is expected to be in the range of 7%-8% of adjusted revenue in FY27.

NEW
FY27 CapEx around INR 2,000 crore

Capital expenditure for FY27 is guided at approximately INR 2,000 crore, primarily for biosimilars and product-specific investments.

DROPPED
Semaglutide launch in India on March 21, 2026

Dr. Reddy's will launch generic Ozempic (diabetes) in India on March 21, with all strengths including oral Rybelsus.

DROPPED
Canada Semaglutide approval expected by May 2026

Health Canada response expected between end-February and May 2026, with launch preparation underway for Q4 or Q1.

DROPPED
Abatacept U.S. launch expected end of calendar 2026

IV presentation BLA filed December 2025; approval expected around end-2026, with sub-Q filing in July 2026 and launch by Jan/Feb 2028.

DROPPED
Global generics gross margin range 50%-55% post-lenalidomide

From Q4 FY26 onwards, without lenalidomide, global generics and PSAI gross margin expected in 50%-55% range.

NEW RISK
Semaglutide approval delays in Brazil

Brazil approval for semaglutide is delayed by 3-4 months, which could impact FY27 unit sales guidance of 12 million units.

NEW RISK
Lenalidomide shelf-stock adjustment recurrence

A surprise INR 453 crore shelf-stock adjustment hit Q4 revenue; similar customer-driven adjustments could recur.

NEW RISK
U.S. generics price erosion

U.S. generics revenue has been flat despite new launches, indicating significant price erosion that may continue.

NEW RISK
CAR T and partnered asset discontinuation

Impairment of INR 135 crore on CAR T and INR 93 crore on partnered asset (Immutep) highlights R&D pipeline risk.

RISK GONE
Regulatory delays for biosimilars in U.S.

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.

RISK GONE
Lenalidomide revenue cliff from Q4

CEO advised to assume zero lenalidomide revenue from Q4 FY26, which will impact overall revenue and margins.

RISK GONE
Semaglutide pricing pressure and competition

Management expects eventual competition in Canada and other markets, with pricing likely settling at lower end of $20-$70 range.

RISK GONE
SG&A cost growth moderation uncertain

SG&A as % of revenue remains elevated at 30% (ex-one-off); management expects growth to moderate but absolute level may not decline.

🤫 Topics management stopped discussing

Canada Semaglutide approval expected by May 2026

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.

SG&A spend to be 27.5%-28% of sales for FY25

Mentioned in Q1 FY25, Q1 FY26, Q2 FY25, Q3 FY25

R&D investments expected in this range for the full fiscal year.

REVLIMID revenue cliff in January 2026

Mentioned in Q2 FY25, Q2 FY26, Q4 FY25

Revlimid sales are declining faster than expected, with Q3 likely the last quarter of meaningful contribution.

Abatacept BLA submission by end of December 2025

Mentioned in Q2 FY26, Q3 FY25

BLA for abatacept IV will be submitted by end of calendar 2025, with high confidence in approval.

Lenalidomide revenue decline sharper than expected

Mentioned in Q1 FY26, Q3 FY25

Lenalidomide sales expected to drop significantly after Q2 FY26; magnitude depends on pricing and competitor behavior.

Fast read

Guidance and risk preview

Top guidance FY27 gross margin above 50%

Management expects gross margins to improve above 50% in FY27, driven by semaglutide launches and cost improvement programs.

Top risk Semaglutide approval delays in Brazil

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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