Suppliers / Gmh Organics

Gmh Organics

India 197 employees Updated 9 July 2026

Gmh Organics is a finished-dose manufacturer based in India. It appears in 48 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), UZPHARM (UZ) and ARCSA (EC). Its GMP standing is certified by EMA, UZPHARM (UZ) and TMDA (TZ). Customs aggregates show $168K of exports covering 4 molecules to 1 destination in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
48
filings across 3 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

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 41 None
UZPHARM (UZ) 4 1
ARCSA (EC) 3 None
EMA None 3
TMDA (TZ) None 1

Scale

Year Revenue Exports Destinations
2025 Not reported $168K 1
2024 Not reported $117K 2
2022 Not reported $10K 1

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 We do not publish the identity of any buyer.

Questions about Gmh Organics

Does Gmh Organics hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Gmh Organics. It does have 48 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Gmh Organics manufacture?
1 registered site is on record, in India (Baddi). Every site is listed on this page with the register it came from.
Which regulators recognise Gmh Organics's GMP?
Current GMP certificates are on record from EMA, UZPHARM (UZ) and TMDA (TZ). 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