Suppliers / Brawn Laboratories

Brawn Laboratories

India 567 employees 2 duplicate records merged Updated 9 July 2026

Brawn Laboratories is a finished-dose manufacturer based in India. It appears in 284 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), EFDA (ET) and DIGEMAPS (DO). Its GMP standing is certified by NAFDAC (NG), UZPHARM (UZ) and FDA (GH). Customs aggregates show $24.7M of exports covering 1,586 molecules to 40 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
284
filings across 9 regulators

Registered plants

Site FDA FEI
Haryana India, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 122 None
EFDA (ET) 69 None
DIGEMAPS (DO) 26 None
UZPHARM (UZ) 24 1
TMDA (TZ) 12 None
MINSA (CR) 11 None
NAFDAC (NG) None 2
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $4.0M 21
2025 Not reported $24.7M 40
2024 Not reported $33.9M 47
2023 Not reported $28.5M 42

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 We do not publish the identity of any buyer.

Questions about Brawn Laboratories

Does Brawn Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Brawn Laboratories. It does have 284 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Brawn Laboratories manufacture?
1 registered site is on record, in Nigeria (Haryana India). Every site is listed on this page with the register it came from.
Which regulators recognise Brawn Laboratories's GMP?
Current GMP certificates are on record from NAFDAC (NG), UZPHARM (UZ) and FDA (GH). 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