Suppliers / Zhongke Junda Biotechnology (Hangzhou)

Zhongke Junda Biotechnology (Hangzhou)

China Updated 9 July 2026

Zhongke Junda Biotechnology (Hangzhou) 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
Gelatin US FDA 1

Also appears on these molecule pages

Gelatin API

Questions about Zhongke Junda Biotechnology (Hangzhou)

Does Zhongke Junda Biotechnology (Hangzhou) hold a US DMF or a CEP?
Zhongke Junda Biotechnology (Hangzhou) 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 Zhongke Junda Biotechnology (Hangzhou) make?
1 molecule is on record against Zhongke Junda Biotechnology (Hangzhou), including Gelatin. 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

Gelita shares 1 molecule PB Gelatins shares 1 molecule Baotou Dongbao Bio-Tech shares 1 molecule Sichuan Raybo Biotechnology shares 1 molecule Tessenderlo Group 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