Suppliers / Zhejiang Liaoyuan Pharmaceuticals

Zhejiang Liaoyuan Pharmaceuticals

China Updated 9 July 2026

Zhejiang Liaoyuan Pharmaceuticals is an API manufacturer based in China. It holds 6 active US drug master files across a filed portfolio of 6 molecules.

6
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Apixaban US FDA 1
Clopidogrel US FDA 1
Duloxetine US FDA 1
Ferric Carboxymaltose US FDA 1
Ivabradine US FDA 1
Mirtazapine US FDA 1

Also appears on these molecule pages

Ferric Carboxymaltose API Ivabradine API Mirtazapine API Clopidogrel API Duloxetine API Apixaban API

Questions about Zhejiang Liaoyuan Pharmaceuticals

Does Zhejiang Liaoyuan Pharmaceuticals hold a US DMF or a CEP?
Zhejiang Liaoyuan Pharmaceuticals holds 6 active US drug master files. 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 Liaoyuan Pharmaceuticals make?
6 molecules are on record against Zhejiang Liaoyuan Pharmaceuticals, including Apixaban, Clopidogrel, Duloxetine and Ferric Carboxymaltose. 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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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