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AUROPHARMA Diversified 12 Feb 2026

Aurobindo Pharma Limited — Q3 FY26

Aurobindo Pharma reported a strong quarter with PAT of INR 910 crore, supported by improving Pen G yields and a favorable government MIP policy on key antibiotics.

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Revenue ₹8,646 Cr
EBITDA
PAT ₹910 Cr
EBITDA Margin
Duration
Read Time 1 min read

✓ Verified against BSE filing

2-Minute Summary

✦ AI-Generated from Full Transcript

Aurobindo Pharma reported a strong quarter with PAT of INR 910 crore, supported by improving Pen G yields and a favorable government MIP policy on key antibiotics. The company is ramping Pen G production to over 10,000 metric tons annualized, with EBITDA breakeven already achieved. Europe continues double-digit growth, and the U.S. injectables business grew 17% despite the ongoing Eugia warning letter. Management guided for EBITDA margins in the 20-21% range for FY26 and expects meaningful contributions from Dayton and Raleigh facilities from FY27. Key risks include the timing of the Eugia warning letter resolution and potential delays in the Lannett acquisition.

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Quarter Snapshot

Pen G annualized production 10,000 metric tons
+138% vs prior year average

Ramp-up progressing; yields improving consistently; expected to reach 65-70% capacity by March 2026.

U.S. injectable sales growth 17%
+17% YoY

Supported by supply ramp-up and improved service levels; injectable business showing steady improvement.

Europe constant currency growth Low double-digit
Low double-digit YoY

Well ahead of market growth; driven by France, Portugal, Germany, Netherlands; China supply improving.

Pen G capacity utilization target 65-70%
+23-28pp vs 42% prior year average

Ramp-up on track; January 2026 already significantly ramped; MIP policy a positive catalyst.

What Changed vs Last Quarter

Comparing Q3 FY26 vs Q2 FY26
3 new guidance3 dropped4 new risk4 risk resolved
NEW
Pen G production to exceed 10,000 metric tons annualized in next 12 months

Based on current production levels, the company expects to produce more than 10,000 metric tons on an annualized basis over the next 12 months.

NEW
Dayton facility to contribute significantly from FY27

The Dayton facility has transitioned to commercial phase and will begin contributing revenues significantly from FY2027 onwards.

NEW
Lannett acquisition expected to close in Q1 FY27

The acquisition is progressing well with FTC; expected to close in the first quarter of FY2027.

UPDATED
EBITDA margin target of 20-21% for FY26

Management expects to achieve EBITDA margins on the higher side of 20-21% for FY2026, driven by Pen G ramp-up, injectable growth, and cost efficiencies.

DROPPED
Europe to exceed EUR 1 billion annual revenue by FY26 end

European business on track to comfortably surpass EUR 1 billion annual revenue milestone by end of FY26, driven by consistent growth across major markets.

DROPPED
China OSG facility EBITDA breakeven by Q3-Q4 FY26

The OSG facility in China is on track to deliver EBITDA breakeven by Q3-Q4 FY26, with European approval for 10 products and 3 local approvals.

DROPPED
Biosimilar denosumab EU submission in April 2026

Marketing authorization application for denosumab biosimilar to be submitted to EMA in April 2026; FDA submission expected in July quarter of 2026.

NEW RISK
Eugia warning letter resolution uncertainty

Despite procedural observations, the USFDA decision on the warning letter is pending; management is cautiously optimistic but cannot predict outcome.

NEW RISK
6-APA predatory pricing impact

6-APA prices have been below cost of manufacture internationally, causing losses; correction expected by April but timing uncertain.

NEW RISK
Lannett acquisition regulatory delays

FTC approval process is ongoing; any delay or unexpected conditions could impact the timeline and synergies.

NEW RISK
Ramp-up costs from multiple greenfield projects

EBITDA burn from ramping up facilities like Pen G, Dayton, Raleigh, and biosimilars may pressure near-term margins.

RISK GONE
UGF3 reinspection delay

FDA reinspection for UGF3 facility is pending; timeline is uncertain (up to 8 months from September 2025), delaying injectable product launches.

RISK GONE
Pen-G MIP policy uncertainty

Minimum import price (MIP) representation to government is pending; if delayed or denied, Pen-G ramp-up and profitability may be impacted.

RISK GONE
Biosimilar competitive intensity

New FDA draft guidance may lower entry barriers, increasing competition; Aurobindo may be third or later entrant in key products like denosumab.

RISK GONE
High CapEx intensity

H1 CapEx at INR 1,500 crore; ongoing investments in biosimilars, biologics CMO, and Pen-G may pressure cash flows despite unutilized capacities.

🤫 Topics management stopped discussing

Biosimilar omalizumab recruitment delays

Mentioned in Q1 FY25, Q2 FY25, 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 OSG facility EBITDA breakeven by Q3-Q4 FY26

Mentioned in Q1 FY26, Q2 FY26

The OSG facility in China is on track to deliver EBITDA breakeven by Q3-Q4 FY26, with European approval for 10 products and 3 local approvals.

China plant commercialization from Q3 FY25

Mentioned in Q1 FY25, 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.

Dayton OSD plant commercialization in next fiscal

Mentioned in Q3 FY25, Q4 FY25

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

Fast read

Guidance and risk preview

Top guidance EBITDA margin target of 20-21% for FY26

Management expects to achieve EBITDA margins on the higher side of 20-21% for FY2026, driven by Pen G ramp-up, injectable growth, and cost efficien...

Top risk Eugia warning letter resolution uncertainty

Despite procedural observations, the USFDA decision on the warning letter is pending; management is cautiously optimistic but cannot predict outcome.

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