Suppliers / Chongqing Mideco Pharmaceutical

Chongqing Mideco Pharmaceutical

China Updated 9 July 2026

Chongqing Mideco Pharmaceutical is an API manufacturer based in China. It holds 3 active US drug master files and one valid CEP across a filed portfolio of 4 molecules.

3
active US DMFs
1
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Jinfeng Town, China Not on file

What they file, and where

Molecule Regulators Docs
Carfilzomib US FDA 1
Ixazomib US FDA 1
Sapropterin US FDA 1
Zinc EDQM 1

Also appears on these molecule pages

Carfilzomib API

Questions about Chongqing Mideco Pharmaceutical

Does Chongqing Mideco Pharmaceutical hold a US DMF or a CEP?
Chongqing Mideco Pharmaceutical holds 3 active US drug master files 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 Chongqing Mideco Pharmaceutical manufacture?
1 registered site is on record, in China (Jinfeng Town). Every site is listed on this page with the register it came from.
What does Chongqing Mideco Pharmaceutical make?
4 molecules are on record against Chongqing Mideco Pharmaceutical, including Carfilzomib, Ixazomib, Sapropterin and Zinc. 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