Suppliers / Chengdu Yazhong Bio-Pharmaceutical

Chengdu Yazhong Bio-Pharmaceutical

China 5 employees Updated 9 July 2026

Chengdu Yazhong Bio-Pharmaceutical is an API manufacturer based in China. It holds 2 valid CEPs.

0
active US DMFs
2
valid CEPs
1
registered plants
2
filings across 1 regulators

Registered plants

Site FDA FEI
Pengzhou, China Not on file

What they file, and where

Molecule Regulators Docs
Diosmin EDQM 2

Also appears on these molecule pages

Diosmin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None

Questions about Chengdu Yazhong Bio-Pharmaceutical

Does Chengdu Yazhong Bio-Pharmaceutical hold a US DMF or a CEP?
Chengdu Yazhong Bio-Pharmaceutical holds 2 valid CEPs. 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.
Where does Chengdu Yazhong Bio-Pharmaceutical manufacture?
1 registered site is on record, in China (Pengzhou). Every site is listed on this page with the register it came from.
What does Chengdu Yazhong Bio-Pharmaceutical make?
1 molecule is on record against Chengdu Yazhong Bio-Pharmaceutical, including Diosmin. Each links through to that molecule's full manufacturer list.
Where does Chengdu Yazhong Bio-Pharmaceutical file?
Filings are on record with MINSA (CR), 2 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