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View Promises →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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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.
ऑरोबिंदो फार्मा ने वित्त वर्ष 2025 की चौथी तिमाही में शानदार प्रदर्शन किया। कंपनी की कमाई 8,382 करोड़ रुपये रही, जो पिछले साल से 11% ज्यादा है। मुनाफा (EBITDA) 1,792 करोड़ रुपये यानी 21.4% मार्जिन पर रहा। इसकी वजह अमेरिका और यूरोप में बिक्री बढ़ना, कीमतें स्थिर रहना और कच्चे माल की लागत कम होना है। पूरे साल की कमाई 31,724 करोड़ रुपये (+9%) और मुनाफा मार्जिन 20.8% रहा। अमेरिका में दवा बिक्री 13% और यूरोप में 17% बढ़ी। इंजेक्टेबल दवाओं की बिक्री 25% बढ़ी। कंपनी अगले साल 7-9% कमाई बढ़ने की उम्मीद करती है, लेकिन जुलाई 2025 में टैरिफ (आयात शुल्क) की घोषणा से अनिश्चितता है। जोखिमों में पेन-जी प्लांट में आग, अमेरिकी टैरिफ और यूजिया-3 की मंजूरी में देरी शामिल है।
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View Promises →Pen-G plant fire disruption
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Read Transcript →US formulation revenue in constant currency terms for Q4 FY25.
Europe formulation revenue in constant currency terms for Q4 FY25.
Company turned net cash positive in Q4 FY25 from net debt position.
R&D expenditure for FY25 was 5.1% of revenue, mainly for clinical trials.
Management expects revenue growth of 8-9% in FY26, excluding the contribution from transient products like Revlimid.
The company internally aims to keep EBITDA margins at present levels (around 20.8%) for FY26.
The China plant, commercialized in FY25, is expected to contribute revenues in FY26 and turn breakeven or slightly positive.
The US-based OSD plant at Dayton is expected to commence commercial manufacturing in Q2 of FY26.
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.
Following positive CHMP opinions, Filgrastim and Pegfilgrastim expected to launch in EU in Q2 FY26, with revenue bookings starting from that quarter.
A fire incident at the Pen-G facility in Kakinada has halted production; resumption depends on regulatory approvals, impacting FY26 revenue and margin assumptions.
Tariff announcements expected in July 2025 could impact US business; management declined to provide specific guidance until clarity emerges.
Eugia-3 facility remains under FDA remediation; injectable growth is expected to be flat in FY26, with recovery only in FY27.
Revenue from Revlimid will be significantly lower in FY26 as the product faces increased competition and limited remaining supply.
Patent expiry in January 2026 could lead to pricing erosion and market share loss; management acknowledged uncertainty but plans to continue supply post-expiry.
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.
Omalizumab and ophthalmic product trials are delayed; ophthalmic recruitment only 50% and expected to complete in H2 2026, pushing back potential launches.
Potential US tariffs on pharmaceutical imports could impact margins; management believes existing US manufacturing footprint provides mitigation.
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.
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.
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.
Mentioned in Q1 FY24, Q2 FY24
On track to achieve $560 million globally for Eugia Specialities in FY24, driven by injectable growth.
Mentioned in Q1 FY24, Q1 FY25
Pen-G plant faced teething problems in Q1; any further delays could impact margin improvement expectations.
Management expects revenue growth of 8-9% in FY26, excluding the contribution from transient products like Revlimid.
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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