Suppliers / Xuzhou Wanbang Jinqiao Pharma

Xuzhou Wanbang Jinqiao Pharma

China Updated 9 July 2026

Xuzhou Wanbang Jinqiao Pharma is an API manufacturer based in China. It holds 5 active US drug master files across a filed portfolio of 5 molecules.

5
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
China, China 3038199656

What they file, and where

Molecule Regulators Docs
Azilsartan Medoxomil US FDA 1
Deucravacitinib US FDA 1
Mavacamten US FDA 1
Venetoclax US FDA 1
Zavegepant US FDA 1

Also appears on these molecule pages

Azilsartan Medoxomil API Deucravacitinib API Mavacamten API Venetoclax API Zavegepant API

Questions about Xuzhou Wanbang Jinqiao Pharma

Does Xuzhou Wanbang Jinqiao Pharma hold a US DMF or a CEP?
Xuzhou Wanbang Jinqiao Pharma holds 5 active US drug master files. 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.
Is Xuzhou Wanbang Jinqiao Pharma FDA-registered?
One site operated by Xuzhou Wanbang Jinqiao Pharma carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Xuzhou Wanbang Jinqiao Pharma manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Xuzhou Wanbang Jinqiao Pharma make?
5 molecules are on record against Xuzhou Wanbang Jinqiao Pharma, including Azilsartan Medoxomil, Deucravacitinib, Mavacamten and Venetoclax. 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