Suppliers / Beijing Taiyang Pharmaceutical Industry

Beijing Taiyang Pharmaceutical Industry

China 1 employees Updated 9 July 2026

Beijing Taiyang Pharmaceutical Industry is an API manufacturer based in China. It holds one active US drug master file.

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

What they file, and where

Molecule Regulators Docs
Diphenhydramine US FDA 1

Also appears on these molecule pages

Diphenhydramine API

Questions about Beijing Taiyang Pharmaceutical Industry

Does Beijing Taiyang Pharmaceutical Industry hold a US DMF or a CEP?
Beijing Taiyang Pharmaceutical Industry 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 Beijing Taiyang Pharmaceutical Industry make?
1 molecule is on record against Beijing Taiyang Pharmaceutical Industry, including Diphenhydramine. 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability