Suppliers / Shandong Risen-Sun Pharmaceutical

Shandong Risen-Sun Pharmaceutical

China Updated 9 July 2026

Shandong Risen-Sun Pharmaceutical is an API manufacturer based in China. It holds 2 valid CEPs across a filed portfolio of 2 molecules.

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

Registered plants

Site FDA FEI
Taian, China Not on file

What they file, and where

Molecule Regulators Docs
Glycopyrronium EDQM 1
Tiotropium EDQM 1

Also appears on these molecule pages

Tiotropium API Glycopyrronium API

Questions about Shandong Risen-Sun Pharmaceutical

Does Shandong Risen-Sun Pharmaceutical hold a US DMF or a CEP?
Shandong Risen-Sun Pharmaceutical holds 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 Shandong Risen-Sun Pharmaceutical manufacture?
1 registered site is on record, in China (Taian). Every site is listed on this page with the register it came from.
What does Shandong Risen-Sun Pharmaceutical make?
2 molecules are on record against Shandong Risen-Sun Pharmaceutical, including Glycopyrronium and Tiotropium. 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