Sunpharma / Q3-FY25

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Positive2025-02-13Back to SUNPHARMA

Revenue

₹13,675 Cr

verified against source

Revenue YoY

10.5%

reported change

EBITDA

₹4,009 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 delivered a solid Q3 FY25 with consolidated sales of INR 13,437 crore, up 10.5% YoY, driven by strong India (13.8% growth) and emerging markets (10.1% growth). EBITDA margin expanded 120 bps YoY to 29.3%, aided by lower material costs and milestone income. Adjusted PAT grew 24.1% YoY to INR 3,220 crore. Specialty sales rose 24.8% to $370M, with balanced contribution from US and ex-US markets. India business gained 40 bps market share to 8.2%, led by volume and new launches. R&D spend was lower than guided at 6.3% of sales due to clinical trial delays; FY25 R&D guidance trimmed to <7%. Management remains focused on specialty pipeline, including Leqselvi (litigation oral arguments in April) and Antibe acquisition. Key risk: potential US tariff policy changes and FDA compliance issues at Halol facility could impact generics recovery.

Colored figures show movement against the previous available record.

Guidance to track

  • Due to delays in clinical trial initiation, R&D expenditure for FY25 is expected to be below the earlier guidance of 7% of sales.
  • Oral arguments for Leqselvi patent litigation expected in April 2025; if favorable, launch could occur before patent expiry in December 2026.
  • Q3 specialty sales benefited from inventory build at a partner; next quarter sales are expected to be lower excluding milestones.

Risks flagged

  • Potential US tariff changes and new administration policies could impact Sun Pharma's US generics and specialty business.
  • Halol facility remains under FDA scrutiny; reinspection has been invited but not scheduled, delaying new product approvals.
  • If the patent litigation outcome is unfavorable, Leqselvi launch could be delayed until December 2026, impacting specialty growth.
  • Delays in finalizing protocols and starting clinical trials have led to lower R&D spend and may push back pipeline milestones.

Key quotes

  • We will remain opportunistic, but the focus on dermatology and ophthalmology will continue.
  • The growth in specialty, whether looked at quarter-on-quarter, year-on-year, has come from both U.S. and ex-U.S. markets.
  • We have invited the agency to inspect our Halol, but when to inspect is a decision that they take.

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