Kekule Pharma is an API manufacturer based in India. It holds 2 active US drug master files across a filed portfolio of 3 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 15 March 2024 as VAI. Customs aggregates show $7.5M of exports covering 192 molecules to 32 destinations in 2025.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| Sangareddy District, India | 3009261338 |
| Molecule | Regulators | Docs |
|---|---|---|
| Nilutamide | US FDA | 2 |
| Celecoxib | SFDA (Saudi Arabia) | 1 |
| Etoricoxib | SFDA (Saudi Arabia) | 1 |
Also appears on these molecule pages
| Regulator | Filings | GMP certificates |
|---|---|---|
| MINSA (CR) | 1 | None |
| US FDA | None | 1 |
| Year | Revenue | Exports | Destinations |
|---|---|---|---|
| 2026 YTD | Not reported | $1.2M | 14 |
| 2025 | Not reported | $7.5M | 32 |
| 2024 | Not reported | $10.1M | 28 |
| 2023 | Not reported | $8.6M | 31 |
Export figures are customs aggregates. We do not publish the identity of any buyer.
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