Suppliers / Guangzhou Hanfang Pharmaceutical

Guangzhou Hanfang Pharmaceutical

China Updated 9 July 2026

Guangzhou Hanfang Pharmaceutical is an API manufacturer based in China. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file.

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

Registered plants

Site FDA FEI
Guangzhou City, China Not on file

What they file, and where

Molecule Regulators Docs
Vincristine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Vincristine API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Questions about Guangzhou Hanfang Pharmaceutical

Does Guangzhou Hanfang Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Guangzhou Hanfang Pharmaceutical. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Guangzhou Hanfang Pharmaceutical manufacture?
1 registered site is on record, in China (Guangzhou City). Every site is listed on this page with the register it came from.
What does Guangzhou Hanfang Pharmaceutical make?
1 molecule is on record against Guangzhou Hanfang Pharmaceutical, including Vincristine. Each links through to that molecule's full manufacturer list.
Where does Guangzhou Hanfang 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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Sources on this page

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