Suppliers / Huazhong Pharmaceuticals

Huazhong Pharmaceuticals

China Updated 9 July 2026

Huazhong Pharmaceuticals is an API manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 2 molecules.

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

Registered plants

Site FDA FEI
Xiangyang, China Not on file

What they file, and where

Molecule Regulators Docs
Thiamine EDQM 2
Diazepam EDQM 1

Also appears on these molecule pages

Diazepam API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None

Questions about Huazhong Pharmaceuticals

Does Huazhong Pharmaceuticals hold a US DMF or a CEP?
Huazhong Pharmaceuticals holds 3 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Huazhong Pharmaceuticals manufacture?
1 registered site is on record, in China (Xiangyang). Every site is listed on this page with the register it came from.
What does Huazhong Pharmaceuticals make?
2 molecules are on record against Huazhong Pharmaceuticals, including Thiamine and Diazepam. Each links through to that molecule's full manufacturer list.
Where does Huazhong Pharmaceuticals file?
Filings are on record with MINSA (CR), 3 in total.

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