Suppliers / Sovereign Pharma

Sovereign Pharma

India 286 employees 3 duplicate records merged Updated 9 July 2026

Sovereign Pharma is a finished-dose manufacturer based in India. It appears in 4 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET) and BOMRA (BW). Its GMP standing is certified by TMDA (TZ), FDA (GH) and MHRA (UK), among 5 authorities. Customs aggregates show $1.4M of exports covering 45 molecules to 8 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
4
filings across 2 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
DAMAN, India Not on file
Nani daman, Tanzania Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 3 None
BOMRA (BW) 1 None
TMDA (TZ) None 1
FDA (GH) None 1
MHRA (UK) None 1
EMA None 1
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2025 Not reported $1.4M 8
2024 Not reported $1.5M 6
2023 Not reported $363K 5

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 We do not publish the identity of any buyer.

Questions about Sovereign Pharma

Does Sovereign Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sovereign Pharma. It does have 4 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sovereign Pharma manufacture?
2 registered sites are on record, in India and Tanzania (Daman and Nani Daman). Every site is listed on this page with the register it came from.
Which regulators recognise Sovereign Pharma's GMP?
Current GMP certificates are on record from TMDA (TZ), FDA (GH), MHRA (UK), EMA and ANVISA (Brazil). 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