Suppliers / Zhejiang Dongying Pharmaceutical

Zhejiang Dongying Pharmaceutical

China Updated 9 July 2026

Zhejiang Dongying Pharmaceutical is an API manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 3 molecules.

0
active US DMFs
3
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Shaoxing, China Not on file

What they file, and where

Molecule Regulators Docs
Cefprozil EDQM 1
Cefuroxime Axetil EDQM 1
Cefuroxime Sodium Sterile EDQM 1

Also appears on these molecule pages

Cefprozil API Cefuroxime API Cefuroxime Axetil API

Questions about Zhejiang Dongying Pharmaceutical

Does Zhejiang Dongying Pharmaceutical hold a US DMF or a CEP?
Zhejiang Dongying Pharmaceutical holds 3 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 Zhejiang Dongying Pharmaceutical manufacture?
1 registered site is on record, in China (Shaoxing). Every site is listed on this page with the register it came from.
What does Zhejiang Dongying Pharmaceutical make?
3 molecules are on record against Zhejiang Dongying Pharmaceutical, including Cefprozil, Cefuroxime Axetil and Cefuroxime Sodium Sterile. 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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Sources on this page

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