Sunpharma / Q1-FY25

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Positive2024-08-01Back to SUNPHARMA

Revenue

₹12,653 Cr

verified against source

Revenue YoY

6.3%

reported change

EBITDA

₹3,607.6 Cr

latest reported figure

Source

nse xbrl

record provenance

Actual signal trajectory

Where this quarter sits.

source records only
EBITDA (₹ Cr)PositiveWatchNegative
11 actual records
Actual quarterly EBITDA (₹ Cr) trajectoryReported values plotted by quarter. Hover or focus a point for its quarter, value, and source sentiment.Q1 FY24: 3,308 · Watch source sentiment · 2023-08-10Q1 FY24Q2 FY24: 3,179.4 · Watch source sentiment · 2023-11-15Q2 FY24Q3 FY24: 3,476.8 · Positive source sentiment · 2024-01-23Q3 FY24Q4 FY24: 3,035.2 · Watch source sentiment · 2024-05-15Q4 FY24Q1 FY25: 3,607.6 · Positive source sentiment · 2024-08-01Q1 FY25Q2 FY25: 3,939 · Positive source sentiment · 2024-11-14Q2 FY25Q3 FY25: 4,009 · Positive source sentiment · 2025-02-13Q3 FY25Q4 FY25: 3,716.1 · Watch source sentiment · 2025-05-15Q4 FY25Q1 FY26: 4,301.7 · Positive source sentiment · 2025-08-01Q1 FY26Q2 FY26: 4,527.1 · Positive source sentiment · 2025-11-14Q2 FY26Q3 FY26: 4,948.5 · Positive source sentiment · 2026-02-07Q3 FY264,948.53,035.2
Values are taken from the available verified source records; sentiment color is a separate source-read indicator.

Quarter read

What the record says.

Sun Pharma reported a solid Q1 FY25 with consolidated sales of INR 12,524.5 crore (+6.3% YoY) and EBITDA margin expansion of 60 bps to 28.5%. PAT surged 40.2% YoY to INR 2,835.6 crore, aided by lower base and operational leverage. India formulation grew 16.4% YoY to INR 4,144.5 crore, gaining market share to 8.6%. U.S. sales were flat at $466M, with specialty up 14.7% to $266M, driven by Ilumya and other products. Key highlight was FDA approval of Leqselvi for alopecia areata, though a preliminary injunction motion by Incyte may delay launch. Management guided for higher R&D spend in subsequent quarters (8-10% of sales) and expects tax rate to normalize. Risk: Leqselvi launch uncertainty due to litigation could impact near-term specialty growth.

Colored figures show movement against the previous available record.

Guidance to track

  • Management expects R&D investment to increase in subsequent quarters, with full-year guidance of 8-10% of sales.
  • Tax rate expected to rise due to expiry of certain exemptions; should be viewed on an annualized basis.
  • Launch timing of Leqselvi will be governed by court ruling on Incyte's motion; company opposes and seeks early outcome.

Risks flagged

  • Incyte filed a preliminary injunction motion to block Leqselvi launch; outcome uncertain and could delay revenue contribution.
  • Management plans to request FDA re-audit once ready, but no specific timeline provided; pending approvals may impact U.S. generic pipeline.
  • U.S. generic sales were flat sequentially; Revlimid contribution was not large this quarter, and sustainability is uncertain.

Key quotes

  • We are pleased with the first cycle approval of Leqselvi by the U.S. FDA. This validates our team's capability to effectively bring treatments from research and development to approval.
  • We have consciously worked towards improving the realization for prescriptions. And that's working well.
  • I think, especially in the context of the U.S., either a favorable judgment or settlement will always remain an option.

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