Suppliers / Graviti Pharmaceuticals

Graviti Pharmaceuticals

India 560 employees Updated 9 July 2026

Graviti Pharmaceuticals is an API and finished-dose manufacturer based in India. It holds 2 active US drug master files. Its most recent recorded inspection, by US FDA, closed on 3 February 2023 as NAI. Customs aggregates show $60.3M of exports covering 2,467 molecules to 2 destinations in 2025.

2
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 3 February 2023 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Sangareddy, India 3012932394

What they file, and where

Molecule Regulators Docs
Pantoprazole US FDA 2

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 2 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $14.4M 1
2025 Not reported $60.3M 2
2024 Not reported $58.1M 2
2023 Not reported $52.5M 2

Export figures are customs aggregates. We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was NAI, on 3 February 2023.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
Customs aggregates
Export values, molecule and destination counts