Granules India (532482) Q3 24/25 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 24/25 earnings summary
8 Jul, 2026Executive summary
Q3 FY25 was impacted by a voluntary production pause at the Gagillapur facility after a US FDA inspection resulted in six Form 483 observations and an OAI classification; operations resumed in October with 90% of CAPAs completed and closure expected by March 2025.
Leadership was strengthened with new appointments in quality and manufacturing; OAI status does not impact ongoing sales but delays new product approvals from the site.
New product launches and approvals included Lisdexamfetamine and Trazodone Hydrochloride in the US, with expansion into CNS, oncology, and anti-diabetic areas.
Growth strategy is driven by new launches from the US GPI facility, expansion in Europe, and a new greenfield formulation facility at Genome Valley.
Consolidated revenue for Q3 FY25 was Rs 11,376.95 million, down year-over-year.
Financial highlights
Q3 FY25 revenue was INR 11,377 million, down 2% year-over-year but up 18% sequentially from Q2 FY25.
Gross margin improved to 61.7% from 57% year-over-year; EBITDA for Q3 FY25 was INR 2,303 million (20.2% margin), down from INR 2,505 million (21.7%) year-over-year.
PAT for Q3 FY25 was Rs. 1,176 million, a 6% decrease year-over-year but a 21% increase sequentially.
R&D spend for the quarter was INR 568 million, up from INR 468 million year-over-year.
Net debt stood at INR 8,289 million, with a cash-to-cash cycle of 213 days and DSO at 76 days.
CapEx for the quarter was INR 1,335 million, mainly for Granules Life Sciences.
ROC for Q3 FY25 was 16.4%.
Cash flow from operations for Q3 FY25 was INR 1,315 million.
Outlook and guidance
Long-term revenue CAGR expected to remain above 20%, with FY26 projected to see around 20% growth aided by new capacity and product launches.
EBITDA margin guidance in the 20–22% range, with gross margins expected to improve as one-off costs subside.
Near-term growth to be driven by new launches from the GPI site and commercialization from the Genome Valley facility.
Some new product launches delayed due to OAI status, but four to five launches from GPI will proceed as planned.
Continued R&D investments and higher regulatory expenses may impact margins in the near term.
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