Suppliers / Weihai Disu Pharmaceutical

Weihai Disu Pharmaceutical

China 16 employees Updated 9 July 2026

Weihai Disu Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file across a filed portfolio of 2 molecules.

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

What they file, and where

Molecule Regulators Docs
Alogliptin SFDA (Saudi Arabia) 1
Solifenacin Succinate US FDA 1

Also appears on these molecule pages

Alogliptin API Solifenacin API

Questions about Weihai Disu Pharmaceutical

Does Weihai Disu Pharmaceutical hold a US DMF or a CEP?
Weihai Disu Pharmaceutical holds 1 active US drug master file. 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.
What does Weihai Disu Pharmaceutical make?
2 molecules are on record against Weihai Disu Pharmaceutical, including Alogliptin and Solifenacin Succinate. 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