Suppliers / Relax Biotech

Relax Biotech

India 45 employees 2 duplicate records merged Updated 9 July 2026

Relax Biotech is a finished-dose manufacturer based in India. It appears in 119 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), FDA (GH) and UZPHARM (UZ). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $1.7M of exports covering 108 molecules to 9 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
119
filings across 4 regulators

Registered plants

Site FDA FEI
g i d c makarpuraba roda 390 010vadodara, India Not on file
Vadodara Gujarat, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 81 1
FDA (GH) 29 None
UZPHARM (UZ) 8 None
MINSA (CR) 1 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $228K 4
2025 Not reported $1.7M 9
2024 Not reported $1.1M 8
2023 Not reported $1.7M 9

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 We do not publish the identity of any buyer.

Questions about Relax Biotech

Does Relax Biotech hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Relax Biotech. It does have 119 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Relax Biotech manufacture?
2 registered sites are on record, in India and Nigeria (G I D C Makarpuraba Roda 390 010vadodara and Vadodara Gujarat). Every site is listed on this page with the register it came from.
Which regulators recognise Relax Biotech's GMP?
Current GMP certificates are on record from CDSCO (India) and NAFDAC (NG). 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