Aurobindo Pharma / Q2-FY25

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Positive2024-11-11Back to AUROPHARMA

Revenue

₹7,796 Cr

verified against source

Revenue YoY

8%

reported change

EBITDA

₹1,566 Cr

latest reported figure

Source

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record provenance

Actual signal trajectory

Where this quarter sits.

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EBITDA (₹ Cr)PositiveWatchNegative
9 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: 1,151.4 · Positive source sentiment · 2023-08-14Q1 FY24Q2 FY24: 1,403 · Positive source sentiment · 2023-11-09Q2 FY24Q3 FY24: 1,601 · Positive source sentiment · 2024-02-12Q3 FY24Q4 FY24: 1,687 · Positive source sentiment · 2024-05-27Q4 FY24Q2 FY25: 1,566 · Positive source sentiment · 2024-11-11Q2 FY25Q3 FY25: 1,628 · Positive source sentiment · 2025-02-12Q3 FY25Q4 FY25: 1,792 · Positive source sentiment · 2025-05-15Q4 FY25Q1 FY26: 1,603 · Watch source sentiment · 2025-08-14Q1 FY26Q2 FY26: 1,678 · Positive source sentiment · 2025-11-14Q2 FY261,7921,151.4
Values are taken from the available verified source records; sentiment color is a separate source-read indicator.

Quarter read

What the record says.

Aurobindo Pharma delivered a steady Q2 FY25 with revenue of INR 7,796 crore (+8% YoY) and EBITDA margin of 20.1%, despite higher R&D costs and penicillin G ramp-up losses. PAT grew 8.6% YoY to INR 817 crore. Growth was driven by strong volume expansion in US oral generics (+9% YoY to $289M) and robust Europe performance (+19% YoY in INR terms). The injectable business faced supply chain headwinds at Unit 3, but management expects normalization by Q4. Penicillin G is on track for breakeven by Q4 FY25. Management reiterated FY25 EBITDA margin guidance of 21%-22%, implying a stronger H2. Key risks include sustained high R&D spend for biosimilar trials and potential freight cost volatility from Red Sea disruptions.

Colored figures show movement against the previous available record.

Guidance to track

  • Management reiterated internal target for full-year EBITDA margin, implying H2 margins will be higher than H1.
  • Expect to achieve breakeven at the penicillin G facility by Q4 FY25, with positive contribution from FY26.
  • Despite Q1/Q2 slowdown, management expects full-year injectable sales to be around $600M, with a possible 5% variance.
  • Phase III recruitment completed; filing expected in 2025 with commercialization in Europe in 2026.

Risks flagged

  • R&D costs jumped ~INR 70 crore in Q2 due to phase III biosimilar trials; management expects elevated spend for at least four more quarters.
  • Higher freight costs (~INR 30 crore impact) due to Red Sea issues; management expects normalization but uncertainty remains.
  • Injectable sales declined 11% YoY due to voluntary production slowdown at Unit 3; full recovery expected only by Q4, with FDA reinspection likely in FY26 Q3.
  • Phase III recruitment for omalizumab is 3-4 months behind schedule, potentially pushing back filing timelines.

Key quotes

  • We are on track to achieve our internal target of 21%-22% for the full year, which means effectively the second half should be better compared to the first half.
  • The worst is over with respect to Unit 3 is concerned. We expect the production level should come back to normalcy by Q4.
  • We have a fairly large base, and adding substantially to this base requires new product, new form of presentation. We are working on it.

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