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

Azithromycin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None

Questions about Huangshi Shixing Pharmaceutical

Does Huangshi Shixing Pharmaceutical hold a US DMF or a CEP?
Huangshi Shixing Pharmaceutical holds 1 active US drug master file and 1 valid CEP. 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.
Is Huangshi Shixing Pharmaceutical FDA-registered?
One site operated by Huangshi Shixing Pharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Huangshi Shixing Pharmaceutical manufacture?
2 registered sites are on record, in China (Huangshi and China). Every site is listed on this page with the register it came from.
What does Huangshi Shixing Pharmaceutical make?
1 molecule is on record against Huangshi Shixing Pharmaceutical, including Azithromycin. Each links through to that molecule's full manufacturer list.
Where does Huangshi Shixing Pharmaceutical file?
Filings are on record with MINSA (CR), 3 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