Suppliers / Assurgen Pharma

Assurgen Pharma

India 38 employees Updated 9 July 2026

Assurgen Pharma is an API manufacturer based in India. It holds 8 valid CEPs across a filed portfolio of 7 molecules. Its GMP standing is certified by EMA. Customs aggregates show $3.6M of exports covering 39 molecules to 11 destinations in 2025.

0
active US DMFs
8
valid CEPs
2
registered plants
0
filings across 0 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
Visakhapatnam, India Not on file
Lalamkoduru Village, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $532K 5
2025 Not reported $3.6M 11
2024 Not reported $2.3M 9
2023 Not reported $2.4M 13

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 We do not publish the identity of any buyer.

Questions about Assurgen Pharma

Does Assurgen Pharma hold a US DMF or a CEP?
Assurgen Pharma holds 8 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Assurgen Pharma manufacture?
2 registered sites are on record, in India (Visakhapatnam and Lalamkoduru Village). Every site is listed on this page with the register it came from.
What does Assurgen Pharma make?
7 molecules are on record against Assurgen Pharma, including Sodium Valproate, Allopurinol, Oxcarbazepine and Pantoprazole. Each links through to that molecule's full manufacturer list.
Which regulators recognise Assurgen Pharma'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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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