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Dr Reddy's Q2: Lenalidomide Fades, the Margin Follows

Dr Reddy's revenue fell 1.5% in Q2 FY27 as US lenalidomide sales faded; North America fell to ₹2,489 crore and the EBITDA margin to 20.6% from 26.7%.

Dr Reddy's Laboratories had revenue of ₹8,671 crore in the September quarter, down 1.5% from a year earlier. The company is clear about why: "Reported YoY growth declined 1.5% due to lower lenalidomide sales". The fall hit the most profitable part of the business. North America revenue dropped to ₹2,489 crore from ₹3,241 crore, and the EBITDA margin to 20.6% from 26.7%. Underneath, the company reports double-digit growth in what it calls the base business, and recovery from a weak June quarter.

The quarter in numbers

IFRS consolidated Q2 FY27 Q1 FY27 Q2 FY26 Source
Revenue ₹8,671 crore ₹8,071 crore ₹8,805 crore [D]
Gross margin 52.1% 46.5% 54.7% [D]
SG&A, % of revenue 32.4% 35.7% 30.0% [D]
R&D, % of revenue 6.0% 7.1% 7.0% [D]
EBITDA margin 20.6% 12.5% 26.7% [D]
Diluted EPS ₹11.1 ₹5.3 ₹17.3 [D]
RoCE, annualised 9.5% 5.3% 21.9% [D]

EBITDA was ₹1,783 crore and profit attributable to shareholders ₹925 crore, 10.7% of revenue ([D]). June was hit by a ₹240 crore provision for inventory and other costs related to a semaglutide API issue ([D]); against that low base, the September quarter looks much better. Against a year ago, it is clearly worse.

Where the revenue moved

Business Q2 FY27 revenue What the deck says Source
North America ₹2,489 crore "Declined YoY due to lower lenalidomide sales." [D]
Emerging markets ₹2,059 crore growth from launches, acquisitions and favourable forex [D]
India ₹1,851 crore double-digit base-business growth [D]
Europe ₹1,393 crore the exception to double-digit growth [D]

North America fell about 23% (our arithmetic, ₹3,241 crore to ₹2,489 crore). The company says its US base business, excluding lenalidomide, grew 12.4% against 2.1% for the US generics market ([D]). Branded businesses (India, emerging markets and NRT) are now 53% of revenue ([D]).

Moat and margin

Focus moat: the US pipeline. A generics company's moat is the next wave of hard-to-make or first-to-file products. Dr Reddy's lists 77 ANDAs and 3 NDAs pending, including 47 Para IV filings and 27 first-to-files ([D]). In the quarter it got USFDA approval for a rituximab biosimilar, launched sugammadex injection first to market, and had generic semaglutide approved in 10 countries ([D]). Its CDMO arm, Aurigene Pharmaceutical Services, passed $100 million of revenue in 12 months ([D]).

Margin: one product's profits are leaving. Gross margin fell 2.6 points and EBITDA margin 6.1 points from a year ago (our arithmetic), while SG&A rose as a share of revenue. That is what losing a high-margin product looks like: revenue nearly flat, profit down by a third.

Compliance. The deck discloses two new Form 483s after USFDA pre-approval inspections in October, with 2 and 3 observations, at its FTO-11 and FTO-9 formulation plants in Andhra Pradesh, which it will answer in time ([D]). It also says it is "On track to resolve issue associated with semaglutide API, where certain batches were found to be out of specification" ([D]).

MoatSCORE (Moat Screener, first pass): Dr. Reddy's Laboratories 5.23, AMBER+. For comparison, Sun Pharmaceutical 5.03, Cipla 5.57 and Lupin 5.50 ([MS]).

The board appointed Akhil Ravi as Head, API and Services, and a member of the Management Council from 13 November. The filing says he "is a related party to the Company, being the sonin-law of Mr. G V Prasad, Co-Chairman and Managing Director" ([M]).

The bear case

  • The profit gap is large: EPS fell from ₹17.3 to ₹11.1 and RoCE from 21.9% to 9.5% in a year ([D]).
  • Half-year revenue fell 3.5% ([O]), so this is not one weak quarter.
  • Regulatory flags are piling up: two new 483s in October and the semaglutide API batches.
  • A family member of the co-chairman now runs the API and services business.

The case for

  • Base business growth: 12.4% in the US excluding lenalidomide, against a 2.1% market ([D]).
  • Branded markets are now more than half of revenue ([D]).
  • A net cash surplus of ₹2,502 crore ([D]).
  • A deep filing pipeline: 47 Para IV and 27 first-to-file opportunities ([D]).

What to watch

  1. North America revenue after lenalidomide, quarter by quarter.
  2. Responses to the October Form 483s at FTO-11 and FTO-9.
  3. Whether gross margin returns toward the 54.7% of a year ago as semaglutide and biosimilars scale.

Sources


Educational research, not investment advice. Every figure above is drawn from Dr. Reddy's own filings, read from the primary documents on 24 October 2026; derived figures are our arithmetic, labelled as such. MoatSCORE read live from the Moat Screener on 24 October 2026. No buy/sell recommendations, no price targets, no share prices. Moat & Margin is not a SEBI-registered Research Analyst or Investment Adviser.