Suppliers / NCPC Hebei Huamin Pharmaceutical

NCPC Hebei Huamin Pharmaceutical

China 5 duplicate records merged Updated 9 July 2026

NCPC Hebei Huamin Pharmaceutical is an API manufacturer based in China. It holds 2 valid CEPs across a filed portfolio of 2 molecules. Its filings concentrate with NAFDAC (NG), MINSA (CR) and UZPHARM (UZ). Its GMP standing is certified by ANVISA (Brazil), UZPHARM (UZ) and EMA, among 5 authorities.

0
active US DMFs
2
valid CEPs
3
registered plants
20
filings across 5 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
SHIJIAZHUANG, China Not on file
SHIJIAZHUANG, China Not on file
Hebei Province, Nigeria Not on file

What they file, and where

Molecule Regulators Docs
Cefotaxime EDQM 1
Cefuroxime Sodium Sterile EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 8 1
MINSA (CR) 6 None
UZPHARM (UZ) 3 1
JFDA (JO) 2 None
ARCSA (EC) 1 None
ANVISA (Brazil) None 1
EMA None 1
MHRA (UK) None 1

Questions about NCPC Hebei Huamin Pharmaceutical

Does NCPC Hebei Huamin Pharmaceutical hold a US DMF or a CEP?
NCPC Hebei Huamin Pharmaceutical holds 2 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 NCPC Hebei Huamin Pharmaceutical manufacture?
3 registered sites are on record, in China and Nigeria (Shijiazhuang and Hebei Province among others). Every site is listed on this page with the register it came from.
What does NCPC Hebei Huamin Pharmaceutical make?
2 molecules are on record against NCPC Hebei Huamin Pharmaceutical, including Cefotaxime and Cefuroxime Sodium Sterile. Each links through to that molecule's full manufacturer list.
Which regulators recognise NCPC Hebei Huamin Pharmaceutical's GMP?
Current GMP certificates are on record from ANVISA (Brazil), UZPHARM (UZ), EMA, NAFDAC (NG) and MHRA (UK). 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