Suppliers / Avik Pharmaceutical

Avik Pharmaceutical

India 103 employees Updated 9 July 2026

Avik Pharmaceutical is an API and finished-dose manufacturer based in India. It holds 8 valid CEPs across a filed portfolio of 8 molecules. Its filings concentrate with MINSA (CR) and CDSCO (India). Its GMP standing is certified by CDSCO (India) and EMA. Customs aggregates show $3.9M of exports covering 237 molecules to 38 destinations in 2025.

0
active US DMFs
8
valid CEPs
3
registered plants
9
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
Vapi, India Not on file
g i d c vapi 396 195 valsad, India Not on file
G.I.D.C., India Not on file

What they file, and where

Molecule Regulators Docs
Prednisolone EDQM, SFDA (Saudi Arabia) 3
Mometasone Furoate EDQM 2
Beclomethasone Dipropionate EDQM 1
Betamethasone Dipropionate SFDA (Saudi Arabia) 1
Budesonide EDQM 1
Clobetasol Propionate EDQM 1
Clobetasone Butyrate EDQM 1
Triamcinolone Acetonide EDQM 1

Also appears on these molecule pages

Beclomethasone API Betamethasone API Budesonide API Clobetasol API Mometasone API Nimodipine finished dose Prednisolone API Triamcinolone Acetonide API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 8 None
CDSCO (India) 1 2
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.0M 22
2025 Not reported $3.9M 38
2024 Not reported $2.9M 35
2023 Not reported $1.7M 23

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 We do not publish the identity of any buyer.

Questions about Avik Pharmaceutical

Does Avik Pharmaceutical hold a US DMF or a CEP?
Avik Pharmaceutical 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 Avik Pharmaceutical manufacture?
3 registered sites are on record, in India (Vapi, G I D C Vapi 396 195 Valsad and G.i.d.c.). Every site is listed on this page with the register it came from.
What does Avik Pharmaceutical make?
8 molecules are on record against Avik Pharmaceutical, including Prednisolone, Mometasone Furoate, Beclomethasone Dipropionate and Betamethasone Dipropionate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Avik Pharmaceutical's GMP?
Current GMP certificates are on record from CDSCO (India) and 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