Suppliers / Chinoin Pharmaceutical And Chemical Works

Chinoin Pharmaceutical And Chemical Works

Hungary Updated 9 July 2026

Chinoin Pharmaceutical And Chemical Works is an API and finished-dose manufacturer based in Hungary. It appears in 10 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), INFARMED (PT) and RCETH (BY). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
10
filings across 4 regulators

Registered plants

Site FDA FEI
MISKOLC, Hungary Not on file

What they file, and where

Molecule Regulators Docs
Alprostadil SFDA (Saudi Arabia) 1
Latanoprost SFDA (Saudi Arabia) 1
Latanoprostene Bunod SFDA (Saudi Arabia) 1
Tamsolusin SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Alprostadil API Latanoprost API Latanoprostene Bunod API

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 6 None
INFARMED (PT) 2 None
RCETH (BY) 1 None
DIGEMAPS (DO) 1 None
ANVISA (Brazil) None 1

Questions about Chinoin Pharmaceutical And Chemical Works

Does Chinoin Pharmaceutical And Chemical Works hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Chinoin Pharmaceutical And Chemical Works. It does have 10 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Chinoin Pharmaceutical And Chemical Works manufacture?
1 registered site is on record, in Hungary (Miskolc). Every site is listed on this page with the register it came from.
What does Chinoin Pharmaceutical And Chemical Works make?
4 molecules are on record against Chinoin Pharmaceutical And Chemical Works, including Alprostadil, Latanoprost, Latanoprostene Bunod and Tamsolusin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Chinoin Pharmaceutical And Chemical Works's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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