Suppliers / Troikaa Pharmaceuticals

Troikaa Pharmaceuticals

India Updated 9 July 2026

Troikaa Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 146 regulatory filings across 15 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), DAV (Vietnam) and ZAMRA (ZM). Its GMP standing is certified by CDSCO (India), UZPHARM (UZ) and NAFDAC (NG), among 6 authorities. Customs aggregates show $58.9M of exports covering 1,677 molecules to 77 destinations in 2025.

0
active US DMFs
0
valid CEPs
8
registered plants
146
filings across 15 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
Dehradun, Colombia Not on file
DEHRADUN, India Not on file
Dehradun, India Not on file
Ahmedabad, India Not on file
tal sanandahmedabada hmedabad 382 170, India Not on file
ahmedabad 382 110, India Not on file

2 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 26 None
DAV (Vietnam) 25 None
ZAMRA (ZM) 22 None
MINSA (CR) 17 None
UZPHARM (UZ) 14 3
TMDA (TZ) 11 None
CDSCO (India) None 5
NAFDAC (NG) None 3
ANVISA (Brazil) None 2
EMA None 1
MCAZ (ZW) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $13.5M 44
2025 Not reported $58.9M 77
2024 Not reported $48.3M 68
2023 Not reported $48.6M 71

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 We do not publish the identity of any buyer.

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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