Risk Intelligence
EU re-inspection delay
View Risks →Lincoln Pharma delivered a solid Q3 FY26 with revenue of ₹166.3 Cr (+13.5% YoY) and PAT of ₹28.6 Cr (+37.7% YoY), driven by strong export growth and the new cephalosporin (CIFA) block contributing ~₹45 Cr annualized.
✓ Verified against BSE filing
Lincoln Pharma delivered a solid Q3 FY26 with revenue of ₹166.3 Cr (+13.5% YoY) and PAT of ₹28.6 Cr (+37.7% YoY), driven by strong export growth and the new cephalosporin (CIFA) block contributing ~₹45 Cr annualized. EBITDA margin expanded ~100 bps to 23.3%, aided by favorable product mix and operating leverage. Management reiterated the ₹1,000 Cr revenue target (likely by FY28-29) with growth from domestic branded generics, regulated markets (Canada, EU), and potential inorganic acquisitions. R&D spend is set to rise from ~2% to ~3% of sales to support dossier filings. Key risk: EU re-inspection delays could push back regulated market revenue ramp-up.
EU re-inspection delay
View Risks →Full transcript text is available on this route.
Read Transcript →9-month EPS vs full-year FY25 EPS of ₹41.11; on track to exceed FY25 full-year.
New cephalosporin block commenced; expected to reach ₹45 Cr revenue in FY26.
From CDMO/CMO projects; 15-17 products commercialized, 23 signed.
Africa contributes ~40% of export revenue; Latam & SE Asia ~25%.
Long-term target reiterated; may slip by 5-6 months from original FY28 timeline.
EU audit (Hungary) expected in May-June 2026; any delay could postpone regulated market revenue.
View Risks →