Suppliers / Psa Chemicals And Pharmaceuticals

Psa Chemicals And Pharmaceuticals

India Updated 9 July 2026

Psa Chemicals And Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 4 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA. Customs aggregates show $154K of exports covering 1 molecule to 1 destination in 2023.

0
active US DMFs
0
valid CEPs
1
registered plants
4
filings across 1 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
Pithampur, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 4 None
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $247K 3
2023 Not reported $154K 1
2022 Not reported $295K 1

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 We do not publish the identity of any buyer.

Questions about Psa Chemicals And Pharmaceuticals

Does Psa Chemicals And Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Psa Chemicals And Pharmaceuticals. It does have 4 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Psa Chemicals And Pharmaceuticals manufacture?
1 registered site is on record, in India (Pithampur). Every site is listed on this page with the register it came from.
Which regulators recognise Psa Chemicals And Pharmaceuticals'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