Suppliers / Zhejiang Candorly Pharmaceutical

Zhejiang Candorly Pharmaceutical

China Updated 9 July 2026

Zhejiang Candorly Pharmaceutical is an API manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Taiping, Wenling City, China Not on file

What they file, and where

Molecule Regulators Docs
Clindamycin US FDA 1
Tenofovir Disoproxil US FDA 1

Also appears on these molecule pages

Clindamycin API Tenofovir Disoproxil API

Questions about Zhejiang Candorly Pharmaceutical

Does Zhejiang Candorly Pharmaceutical hold a US DMF or a CEP?
Zhejiang Candorly Pharmaceutical holds 2 active US drug master files. 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 Candorly Pharmaceutical manufacture?
1 registered site is on record, in China (Taiping, Wenling City). Every site is listed on this page with the register it came from.
What does Zhejiang Candorly Pharmaceutical make?
2 molecules are on record against Zhejiang Candorly Pharmaceutical, including Clindamycin and Tenofovir Disoproxil. 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