Hebei Meihe Pharmaceutical
Updated 9 July 2026
Hebei Meihe Pharmaceutical is an API manufacturer. It holds one active US drug master file.
1
filings
across 1 regulators
What they file, and where
Also appears on these molecule pages
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| MINSA (CR) | 1 | None |
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Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability