Suppliers / Hebei Jiheng Group Pharmaceutical

Hebei Jiheng Group Pharmaceutical

China Updated 9 July 2026

Hebei Jiheng Group Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file. Its filings concentrate with MINSA (CR) and ARCSA (EC).

1
active US DMFs
0
valid CEPs
0
registered plants
7
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Acetaminophen US FDA 1

Also appears on these molecule pages

Acetaminophen API Paracetamol API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 5 None
ARCSA (EC) 2 None

Questions about Hebei Jiheng Group Pharmaceutical

Does Hebei Jiheng Group Pharmaceutical hold a US DMF or a CEP?
Hebei Jiheng Group Pharmaceutical holds 1 active US drug master file. 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.
What does Hebei Jiheng Group Pharmaceutical make?
1 molecule is on record against Hebei Jiheng Group Pharmaceutical, including Acetaminophen. Each links through to that molecule's full manufacturer list.
Where does Hebei Jiheng Group Pharmaceutical file?
Filings are on record with MINSA (CR) and ARCSA (EC), 7 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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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