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 We do not publish the identity of any buyer.

Questions about Ratnatris Pharmaceuticals

Does Ratnatris Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ratnatris Pharmaceuticals. It does have 24 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Ratnatris Pharmaceuticals manufacture?
3 registered sites are on record, in India and Nigeria (Mehsana and Mehsana 382 715 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Ratnatris Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India), ZAMRA (ZM), TMDA (TZ) and NAFDAC (NG). 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