Suppliers / Hebei Meihe Pharmaceutical

Hebei Meihe Pharmaceutical

China Updated 9 July 2026

Hebei Meihe Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file.

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

What they file, and where

Molecule Regulators Docs
Ivermectin US FDA 1

Also appears on these molecule pages

Ivermectin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Questions about Hebei Meihe Pharmaceutical

Does Hebei Meihe Pharmaceutical hold a US DMF or a CEP?
Hebei Meihe 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 Meihe Pharmaceutical make?
1 molecule is on record against Hebei Meihe Pharmaceutical, including Ivermectin. Each links through to that molecule's full manufacturer list.
Where does Hebei Meihe Pharmaceutical file?
Filings are on record with MINSA (CR), 1 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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Comparable suppliers

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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