Suppliers / Zhejiang Fengrun Biotech

Zhejiang Fengrun Biotech

China Updated 9 July 2026

Zhejiang Fengrun Biotech is an API manufacturer based in China. It holds one active US drug master file.

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

What they file, and where

Molecule Regulators Docs
Glucosamine US FDA 1

Also appears on these molecule pages

Glucosamine API

Questions about Zhejiang Fengrun Biotech

Does Zhejiang Fengrun Biotech hold a US DMF or a CEP?
Zhejiang Fengrun Biotech holds 1 active US drug master file. 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.
What does Zhejiang Fengrun Biotech make?
1 molecule is on record against Zhejiang Fengrun Biotech, including Glucosamine. Each links through to that molecule's full manufacturer list.

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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Comparable suppliers

Zhejiang Cheng Yi Pharmaceutical shares 1 molecule Zhejiang Golden-Shell Pharmaceutical shares 1 molecule Meck Pharmaceuticals And Chemicals shares 1 molecule Zhejiang Zhoushan Putuo Xinxing Pharmas shares 1 molecule

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