Suppliers / Teva API India

Teva API India

India 3 duplicate records merged Updated 9 July 2026

Teva API India is an API manufacturer based in India. Its GMP standing is certified by EMA. Customs aggregates show $109.5M of exports covering 2,022 molecules to 40 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Gajraula, India Not on file
Bhind, India Not on file

What they file, and where

Molecule Regulators Docs
Caspofungin SFDA (Saudi Arabia) 2
Irbesartan SFDA (Saudi Arabia) 2

Also appears on these molecule pages

Caspofungin API Irbesartan API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $15.6M 26
2025 Not reported $109.5M 40
2024 Not reported $116.8M 43
2023 Not reported $111.5M 38

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 We do not publish the identity of any buyer.

Questions about Teva API India

Where does Teva API India manufacture?
2 registered sites are on record, in India (Gajraula and Bhind). Every site is listed on this page with the register it came from.
What does Teva API India make?
2 molecules are on record against Teva API India, including Caspofungin and Irbesartan. Each links through to that molecule's full manufacturer list.
Which regulators recognise Teva API India's GMP?
Current GMP certificates are on record from EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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