Suppliers / Zhejiang Taizhou Hisyn Pharmaceutical

Zhejiang Taizhou Hisyn Pharmaceutical

China Updated 9 July 2026

Zhejiang Taizhou Hisyn Pharmaceutical is an API manufacturer based in China. It holds 4 valid CEPs across a filed portfolio of 3 molecules.

0
active US DMFs
4
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Linhai, China Not on file
Taizhou, China Not on file

What they file, and where

Molecule Regulators Docs
Iohexol EDQM 2
Iopamidol EDQM 2
Iodixanol SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Questions about Zhejiang Taizhou Hisyn Pharmaceutical

Does Zhejiang Taizhou Hisyn Pharmaceutical hold a US DMF or a CEP?
Zhejiang Taizhou Hisyn Pharmaceutical holds 4 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 Taizhou Hisyn Pharmaceutical manufacture?
2 registered sites are on record, in China (Linhai and Taizhou). Every site is listed on this page with the register it came from.
What does Zhejiang Taizhou Hisyn Pharmaceutical make?
3 molecules are on record against Zhejiang Taizhou Hisyn Pharmaceutical, including Iohexol, Iopamidol and Iodixanol. 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