Suppliers / Sotac Pharmaceuticals

Sotac Pharmaceuticals

India 64 employees Updated 9 July 2026

Sotac Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 7 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ) and ARCSA (EC). Its GMP standing is certified by CDSCO (India). Customs aggregates show $0 of exports covering 1 molecule to 1 destination in 2024.

0
active US DMFs
0
valid CEPs
1
registered plants
7
filings across 2 regulators

Registered plants

Site FDA FEI
sanand 382 110ahmedabad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 6 None
ARCSA (EC) 1 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2024 Not reported $0 1
2022 Not reported $1K 2

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 We do not publish the identity of any buyer.

Questions about Sotac Pharmaceuticals

Does Sotac Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sotac Pharmaceuticals. It does have 7 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sotac Pharmaceuticals manufacture?
1 registered site is on record, in India (Sanand 382 110ahmedabad). Every site is listed on this page with the register it came from.
Which regulators recognise Sotac Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India). 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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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