Suppliers / Zhejiang Dongbang Pharmaceutical

Zhejiang Dongbang Pharmaceutical

China Updated 9 July 2026

Zhejiang Dongbang Pharmaceutical is an API manufacturer based in China. It holds one valid CEP. Its GMP standing is certified by MFDS (Korea).

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

Registered plants

Site FDA FEI
Taizhou, China Not on file

What they file, and where

Molecule Regulators Docs
Cefaclor EDQM 1

Also appears on these molecule pages

Cefaclor API

Filings and GMP by regulator

Regulator Filings GMP certificates
MFDS (Korea) None 2

Questions about Zhejiang Dongbang Pharmaceutical

Does Zhejiang Dongbang Pharmaceutical hold a US DMF or a CEP?
Zhejiang Dongbang Pharmaceutical holds 1 valid CEP. 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 Dongbang Pharmaceutical manufacture?
1 registered site is on record, in China (Taizhou). Every site is listed on this page with the register it came from.
What does Zhejiang Dongbang Pharmaceutical make?
1 molecule is on record against Zhejiang Dongbang Pharmaceutical, including Cefaclor. Each links through to that molecule's full manufacturer list.
Which regulators recognise Zhejiang Dongbang Pharmaceutical's GMP?
Current GMP certificates are on record from MFDS (Korea). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates