Suppliers / Pharmaresources (Kaiyuan)

Pharmaresources (Kaiyuan)

China Updated 9 July 2026

Pharmaresources (Kaiyuan) is an API manufacturer based in China. It holds 5 active US drug master files and 2 valid CEPs across a filed portfolio of 2 molecules.

5
active US DMFs
2
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Kaiyuan City, China Not on file

What they file, and where

Molecule Regulators Docs
Ticagrelor EDQM, US FDA 5
Levocarnitine EDQM, US FDA 2

Also appears on these molecule pages

Levocarnitine API Ticagrelor contract manufacturing

Questions about Pharmaresources (Kaiyuan)

Does Pharmaresources (Kaiyuan) hold a US DMF or a CEP?
Pharmaresources (Kaiyuan) holds 5 active US drug master files and 2 valid CEPs. 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 Pharmaresources (Kaiyuan) manufacture?
1 registered site is on record, in China (Kaiyuan City). Every site is listed on this page with the register it came from.
What does Pharmaresources (Kaiyuan) make?
2 molecules are on record against Pharmaresources (Kaiyuan), including Ticagrelor and Levocarnitine. 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