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AUROPHARMA Diversified 15 May 2025

Aurobindo Pharma Limited — Q4 FY25

Aurobindo Pharma delivered a strong Q4 FY25 with revenue of INR 8,382 crore (+11% YoY) and EBITDA of INR 1,792 crore (21.4% margin), driven by volume growth in US and Europe, stable pricing, and easing raw material costs.

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Revenue ₹8,382 Cr +11%
EBITDA ₹1,792 Cr +6%
PAT ₹903 Cr
EBITDA Margin 21.4%
Duration
Read Time 1 min read

✓ Verified against BSE filing

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Aurobindo Pharma delivered a strong Q4 FY25 with revenue of INR 8,382 crore (+11% YoY) and EBITDA of INR 1,792 crore (21.4% margin), driven by volume growth in US and Europe, stable pricing, and easing raw material costs. Full-year revenue reached INR 31,724 crore (+9% YoY) with EBITDA margin expanding to 20.8%. US formulation grew 13% YoY to INR 4,072 crore, Europe grew 17% to INR 2,147 crore, and the injectable business rose 25% YoY. Management guided for high single-digit revenue growth in FY26 (excluding transient products) and aims to maintain current EBITDA margins, though tariff announcements in July 2025 add uncertainty. Key risks include the Pen-G plant fire disruption, potential US tariffs, and muted injectable growth in FY26 pending FDA clearance of Eugia-3.

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Quarter Snapshot

US Formulation Revenue (constant currency) $470M
+9% YoY

US formulation revenue in constant currency terms for Q4 FY25.

Europe Formulation Revenue (constant currency) €236M
+16% YoY

Europe formulation revenue in constant currency terms for Q4 FY25.

Net Cash Position $42M
from net debt of $84M in Dec 2024

Company turned net cash positive in Q4 FY25 from net debt position.

R&D Spend as % of Revenue 5.1%
flat YoY

R&D expenditure for FY25 was 5.1% of revenue, mainly for clinical trials.

What Changed vs Last Quarter

Comparing Q4 FY25 vs Q3 FY25
2 new guidance2 dropped4 new risk4 risk resolved
NEW
High single-digit revenue growth in FY26 excluding transient products

Management expects revenue growth of 8-9% in FY26, excluding the contribution from transient products like Revlimid.

NEW
Maintain current EBITDA margins in FY26

The company internally aims to keep EBITDA margins at present levels (around 20.8%) for FY26.

UPDATED
China OSD plant to contribute revenues in FY26

The China plant, commercialized in FY25, is expected to contribute revenues in FY26 and turn breakeven or slightly positive.

UPDATED
US Dayton OSD plant commercialization in Q2 FY26

The US-based OSD plant at Dayton is expected to commence commercial manufacturing in Q2 of FY26.

DROPPED
FY25 EBITDA margin guidance of 21%-22%

Management reaffirmed achieving 21%-22% EBITDA margin for FY25, despite Q3 margin of 20.4%, citing stronger Q4 with increased transient sales and operational efficiencies.

DROPPED
Biosimilar launches in EU from July 2025

Following positive CHMP opinions, Filgrastim and Pegfilgrastim expected to launch in EU in Q2 FY26, with revenue bookings starting from that quarter.

NEW RISK
Pen-G plant fire disruption

A fire incident at the Pen-G facility in Kakinada has halted production; resumption depends on regulatory approvals, impacting FY26 revenue and margin assumptions.

NEW RISK
Potential US tariffs on pharmaceutical imports

Tariff announcements expected in July 2025 could impact US business; management declined to provide specific guidance until clarity emerges.

NEW RISK
Muted injectable growth in FY26 due to Eugia-3 remediation

Eugia-3 facility remains under FDA remediation; injectable growth is expected to be flat in FY26, with recovery only in FY27.

NEW RISK
Revlimid revenue decline in FY26

Revenue from Revlimid will be significantly lower in FY26 as the product faces increased competition and limited remaining supply.

RISK GONE
Generic Revlimid patent expiry impact

Patent expiry in January 2026 could lead to pricing erosion and market share loss; management acknowledged uncertainty but plans to continue supply post-expiry.

RISK GONE
Eugia injectables capacity ramp-up delays

Capacity utilization at Eugia remains at 50% due to supply challenges; any further delays in returning to normal run-rate could impact US injectable revenue.

RISK GONE
Biosimilar clinical trial delays

Omalizumab and ophthalmic product trials are delayed; ophthalmic recruitment only 50% and expected to complete in H2 2026, pushing back potential launches.

RISK GONE
US tariff risk on pharmaceuticals

Potential US tariffs on pharmaceutical imports could impact margins; management believes existing US manufacturing footprint provides mitigation.

🤫 Topics management stopped discussing

FY24 EBITDA margin target of 18%+ (ex-Revlimid)

Mentioned in Q1 FY24, Q1 FY25, Q2 FY24, Q2 FY25, Q3 FY24, Q4 FY24

Management reiterated internal target for full-year EBITDA margin, implying H2 margins will be higher than H1.

Biosimilar omalizumab recruitment delays

Mentioned in Q1 FY25, Q2 FY25, Q3 FY24, Q3 FY25

Omalizumab and ophthalmic product trials are delayed; ophthalmic recruitment only 50% and expected to complete in H2 2026, pushing back potential launches.

China plant revenue generation from Q1/Q2 FY25

Mentioned in Q1 FY25, Q3 FY24, Q3 FY25

The China OSD plant (2B units capacity) commercialized in November 2024, expected to ramp up and contribute to revenues in FY26, initially supplying Europe.

Eugia Specialities global revenue of $560 million for FY24

Mentioned in Q1 FY24, Q2 FY24

On track to achieve $560 million globally for Eugia Specialities in FY24, driven by injectable growth.

PLI Pen-G ramp-up delays

Mentioned in Q1 FY24, Q1 FY25

Pen-G plant faced teething problems in Q1; any further delays could impact margin improvement expectations.

Fast read

Guidance and risk preview

Top guidance High single-digit revenue growth in FY26 excluding transient products

Management expects revenue growth of 8-9% in FY26, excluding the contribution from transient products like Revlimid.

Top risk Pen-G plant fire disruption

A fire incident at the Pen-G facility in Kakinada has halted production; resumption depends on regulatory approvals, impacting FY26 revenue and mar...

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