Date: November 02, 2026
Financial Performance Summary
Quarterly Consolidated Financials (All numbers in INR Mn)
| Metric | Q2FY27 | Q1FY27 | QoQ Growth | Q2FY26 | YoY Growth |
| Revenue from Operations | 15,600 | 14,768 | 6% | 12,970 | 20% |
| EBITDA | 3,376 | 3,389 | 0% | 2,782 | 21% |
| EBITDA % | 22% | 23% | - | 21% | - |
| PBT | 2,434 | 2,404 | 1% | 1,759 | 38% |
| PAT | 1,818 | 1,800 | 1% | 1,306 | 39% |
| PAT % | 12% | 12% | - | 10% | - |
Business Performance Highlights
Revenue Breakdown by Geography:
- North America contributed 72% of revenue in Q2FY27 (compared to 76% in Q2FY26)
- Europe contributed 16% of revenue in Q2FY27 (compared to 12% in Q2FY26)
Revenue Breakdown by Business Segment:
- Finished Dosages (FD): 73% of revenue
- Active Pharmaceuticals Ingredients (API): 13% of revenue
- Pharmaceutical Formulation Intermediates (PFI): 10% of revenue
- Peptides CDMO: 3% of revenue
Financial Metrics:
- Return on Capital Employed (ROCE): 17.6% in Q2FY27 (in line with FY26)
- Net cash position: ₹8,280 million at quarter end (compared to net debt of ₹1,012 million in Q1 FY27)
Management Commentary
Dr. Krishna Prasad Chigurupati, Chairman & Managing Director, commented:
- Quarterly revenue crossed ₹1,500 Cr in Q2 FY27 with EBITDA of ₹338 Cr
- Despite higher input and logistics costs from tensions in West Asia
- Cost pressures will persist and company is working with customers to manage them with a lag
- Filed two potential first-to-file ANDAs in H1, making a total of three potential first-to-file ANDAs
- Company continues to shift towards complex generics and peptide CDMO
- With balance warrant proceeds received, company holds net cash of ₹828 Cr to invest in R&D, manufacturing and quality
Regulatory Update
- Recently concluded a US FDA audit at the Gagillapur site
- The inspection progressed constructively
- Observations are of a nature that can be fully addressed through responses and corrective and preventive actions
- Company will continue to engage transparently with the agency
Company Background
Granules India Limited is a vertically integrated pharmaceutical company:
- Incorporated in 1991, headquartered in Hyderabad
- Present across entire value chain: APIs, PFIs, FDs, and Peptides CDMO
- Products distributed to over 300+ customers in regulated and semi-regulated markets
- Global presence in over 80+ countries with offices in India, US, and UK
- 10 manufacturing facilities (7 in India, 2 in USA, 1 in Switzerland)
- Regulatory approvals from US FDA, EDQM, EU GMP, COFEPRIS, WHO GMP, TGA, K FDA, DEA, MCC and HALAL