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2026-07-22 09:40:28 am | Source: Motilal Oswal Financial Services Ltd Ltd
Buy Granules India for the Target Rs 1,010 by Motilal Oswal Financial Services Ltd
Buy Granules India for the Target Rs 1,010 by Motilal Oswal Financial Services Ltd

FDF/API drive earnings Strong start to FY27; complex generics lead the way

* Granules India (GRAN) delivered in-line revenue/EBITDA/PAT in 1QFY27. Higher formulation (FDF) and API sales sustained growth momentum in 1QFY27 as well. Notably, 1QFY27 was the fifth consecutive quarter of healthy YoY growth in earnings.

* CDMO business remained in the ramp-up phase, with revenue of INR600m in 1QFY27. Due to changes in project milestone services, GRAN reported an EBITDA loss of INR24m in 1QFY27.

* The growth in Europe (+50% YoY) was driven by API/FDF, supported by products/dossiers filed in prior periods.

* The complex generics revenue share has increased considerably from 39% YoY to 50% for 1QFY27. GRAN remains on track to shift from a volumedriven to a value-driven complex-Gx-led business model.

* GRAN is enhancing its prospects in the CDMO segment by adding solidphase peptide synthesis and lyophilization capabilities at its Zurich facility.

* Notably, CFO increased to INR3.8b in 1QFY27, aided by lower receivable days in the US segment.

* We raise our earnings estimates by 1.0%/1.2% for FY27/FY28, factoring in: 

a) increased off-take of complex-Gx products

b) the scale-up of CDMO peptide business

c) improved API sales

d) better operating leverage. We value GRAN at 23x 12-month forward earnings to arrive at our TP of INR1,010. Reiterate BUY.

Gagillapur re-inspection outcome awaited

* In 1QFY27, GRAN’s GPI facility in Virginia received USFDA clearance in Jun’26.

* Consequently, seven of its eight facilities now have a clean EIR, with Gagillapur being the only facility awaiting regulatory resolution. Management indicated that remediation at Gagillapur is complete and responses have been submitted to the USFDA on time.

* Operations/supplies from Gagillapur remain unaffected. However, nine ANDAs pending for approvals are subject to successful USFDA inspections.

* Collectively, these developments reflect material progress in strengthening regulatory compliance and transitioning toward a more stable and audit-ready operating environment.

 

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