Suppliers / Hof Pharmaceuticals

Hof Pharmaceuticals

India 81 employees Updated 9 July 2026

Hof Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 17 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), FDA (GH) and DIGEMAPS (DO). Its GMP standing is certified by CDSCO (India) and FDA (GH). Customs aggregates show $597K of exports covering 80 molecules to 4 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
17
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Ahmedabad, India 3023491920
Ahmedabad, India Not on file
ahmedabad 382 110, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 7 None
FDA (GH) 5 1
DIGEMAPS (DO) 2 None
ARCSA (EC) 2 None
CDSCO (India) 1 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $73K 1
2025 Not reported $597K 4
2024 Not reported $139K 4
2023 Not reported $38K 1

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 We do not publish the identity of any buyer.

Questions about Hof Pharmaceuticals

Does Hof Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Hof Pharmaceuticals. It does have 17 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Hof Pharmaceuticals FDA-registered?
One site operated by Hof Pharmaceuticals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Hof Pharmaceuticals manufacture?
3 registered sites are on record, in India (Ahmedabad and Ahmedabad 382 110 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Hof Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India) 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