Suppliers / Huangshi Shixing Pharmaceutical

Huangshi Shixing Pharmaceutical

China Updated 9 July 2026

Huangshi Shixing Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file and one valid CEP.

1
active US DMFs
1
valid CEPs
2
registered plants 1 with an FDA FEI number
3
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Huangshi, China Not on file
China, China 3033274771

What they file, and where

Molecule Regulators Docs
Azithromycin EDQM, US FDA 2

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability