Aurobindo Pharma / Q4-FY24

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Positive2024-05-27Back to AUROPHARMA

Revenue

₹7,580 Cr

verified against source

Revenue YoY

17%

reported change

EBITDA

₹1,687 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 strong Q4 FY24 with revenue of INR 7,850 crore (+17% YoY) and EBITDA of INR 1,687 crore (+68% YoY), driven by volume gains, new product launches, stable pricing, and raw material cost softening. EBITDA margin expanded 680 bps YoY to 22.3%, while PAT grew 80% to INR 909 crore. US formulation revenue rose 22% to INR 3,588 crore, and Europe grew 10% to INR 1,832 crore. Management guided for FY25 EBITDA margin of 21%-22%, supported by ramp-up of Pen-G and 6-APA facilities, though Eugia 3's OAI status poses a near-term risk to injectable growth. Biosimilar pipeline advances with trastuzumab filing in US expected within 3 months. Key risk: Eugia 3 remediation may delay approvals and impact injectable revenue trajectory.

Colored figures show movement against the previous available record.

Guidance to track

  • Management expects EBITDA margin to improve to 21%-22% in FY25, driven by operating leverage and ramp-up of new capacities.
  • Pen-G and 6-APA facilities will start meaningful contribution from Q3 FY25, with full ramp-up expected by September 2024.
  • Eugia expects to maintain a global revenue run rate of $150 million per year, with US contributing $100-$110 million.
  • Trastuzumab biosimilar to be filed with US FDA within the next 3 months, following a successful Type 4 pre-submission meeting.

Risks flagged

  • Eugia 3 plant classified as OAI; 29 pending ANDAs may be stuck for at least 1 year, impacting injectable growth.
  • Management expects meaningful biosimilar revenue only by 2027-2028, later than some investor expectations.
  • Pen-G fermentation is complex; yield optimization will only be addressed by September, posing execution risk.
  • Management is conservative on Ryzneuta (pegfilgrastim biosimilar) launch, citing multiple competitors and uncertain pricing.

Key quotes

  • We expect to achieve around a 21%-22% EBITDA margin target set internally for the year.
  • I am very optimistic about a product like Omalizumab, where we will be probably one of the four companies to vie for the U.S. and the European market.
  • We have taken whatever sales hit what we wanted to taken in Q4 of last year, okay? Now, Q1 onwards, it should be normal.

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