Suppliers / Ratnatris Pharmaceuticals

Ratnatris Pharmaceuticals

India 2 duplicate records merged Updated 9 July 2026

Ratnatris Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 24 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC) and NAFDAC (NG). Its GMP standing is certified by CDSCO (India), ZAMRA (ZM) and TMDA (TZ), among 4 authorities. Customs aggregates show $314K of exports covering 49 molecules to 7 destinations in 2026 so far.

0
active US DMFs
0
valid CEPs
3
registered plants
24
filings across 2 regulators

Registered plants

Site FDA FEI
Mehsana, India Not on file
mehsana 382 715, India Not on file
Mehsana, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 19 None
NAFDAC (NG) 5 1
CDSCO (India) None 2
ZAMRA (ZM) None 1
TMDA (TZ) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $314K 7

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 We do not publish the identity of any buyer.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