Suppliers / Innova Captab

Innova Captab

India 744 employees 5 duplicate records merged Updated 9 July 2026

Innova Captab is a finished-dose manufacturer based in India. It appears in 103 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), EFDA (ET) and ARCSA (EC). Its GMP standing is certified by FDA (GH), NAFDAC (NG) and EMA, among 4 authorities. Customs aggregates show $31.6M of exports covering 2,368 molecules to 27 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
103
filings across 8 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
BADDI, India Not on file
Solan, India Not on file
Solan, Nigeria Not on file
Solan, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 23 2
EFDA (ET) 21 None
ARCSA (EC) 19 None
TMDA (TZ) 17 None
CDSCO (India) 16 None
MINSA (CR) 5 None
FDA (GH) None 2
EMA None 2
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $5.9M 16
2025 Not reported $31.6M 27
2024 Not reported $15.8M 29
2023 Not reported $14.0M 27

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 We do not publish the identity of any buyer.

Questions about Innova Captab

Does Innova Captab hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Innova Captab. It does have 103 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Innova Captab manufacture?
4 registered sites are on record, in India and Nigeria (Baddi and Solan among others). Every site is listed on this page with the register it came from.
Which regulators recognise Innova Captab's GMP?
Current GMP certificates are on record from FDA (GH), NAFDAC (NG), EMA and MHRA (UK). 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