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GRANULES Diversified 10 Feb 2026

Granules India Limited — Q3 FY26

Granules India delivered a strong Q3 FY26 with consolidated revenue of ₹1,388 crore (+22% YoY) and EBITDA of ₹308 crore (+34% YoY), with margins expanding 196 bps YoY to 22.2%.

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Revenue ₹1,388 Cr +22%
EBITDA ₹308 Cr +34%
PAT ₹150 Cr
EBITDA Margin 22.2% +196bps
Duration 45 min
Read Time 1 min read

✓ Verified against BSE filing

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Granules India delivered a strong Q3 FY26 with consolidated revenue of ₹1,388 crore (+22% YoY) and EBITDA of ₹308 crore (+34% YoY), with margins expanding 196 bps YoY to 22.2%. Growth was broad-based, led by formulations in North America and Europe, and a shift toward complex generics (now 49% of sales vs 27% a year ago). The Gagilapur remediation remains on track with a post-warning letter meeting held in January; no concerns raised by FDA. The peptide CDMO business (SLS) posted a ₹25 crore EBITDA loss due to planned maintenance, but management expects a meaningful improvement in Q4 and breakeven. The preferential issue strengthens the balance sheet for capacity expansion. Key risk: any delay in Gagilapur resolution could impact new product launches and US revenue trajectory.

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Risk Intelligence

Gagilapur FDA warning letter resolution timeline uncertain

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Quarter Snapshot

Complex generics share of sales 49%
+22pp YoY

Complex generics contribution rose from 27% in Q3 FY25 to 49% in Q3 FY26, reflecting product mix improvement.

Peptide CDMO revenue (SLS) ₹33 crore
+18% QoQ

Revenue increased from ₹28 crore in Q2 FY26, driven by execution of key customer projects.

Net debt ₹1,015 crore
-0.9% QoQ

Net debt reduced slightly from ₹1,024 crore in Q2 FY26, indicating stable leverage.

Cash conversion cycle 202 days
-2 days QoQ

Improved from 204 days in Q2 FY26, reflecting better working capital management.

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Guidance and risk preview

Top guidance Peptide CDMO to turn EBITDA positive in Q4 FY26

Management expects meaningful improvement in Q4 performance, with the business reaching EBITDA breakeven in the current quarter.

Top risk Gagilapur FDA warning letter resolution timeline uncertain

Management could not provide a timeline for FDA reinspection or final resolution, which may delay new product launches from the site.

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