Suppliers / Zhejiang Zhebei Pharmaceutical

Zhejiang Zhebei Pharmaceutical

China Updated 9 July 2026

Zhejiang Zhebei Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file and one valid CEP.

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

Registered plants

Site FDA FEI
Xinshi Town, Deqing, China Not on file

What they file, and where

Molecule Regulators Docs
Acyclovir EDQM, US FDA 2

Also appears on these molecule pages

Acyclovir API

Questions about Zhejiang Zhebei Pharmaceutical

Does Zhejiang Zhebei Pharmaceutical hold a US DMF or a CEP?
Zhejiang Zhebei Pharmaceutical holds 1 active US drug master file and 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 Zhebei Pharmaceutical manufacture?
1 registered site is on record, in China (Xinshi Town, Deqing). Every site is listed on this page with the register it came from.
What does Zhejiang Zhebei Pharmaceutical make?
1 molecule is on record against Zhejiang Zhebei Pharmaceutical, including Acyclovir. 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