Suppliers / Wanbang Biopharmaceuticals

Wanbang Biopharmaceuticals

China 14 employees Updated 9 July 2026

Wanbang Biopharmaceuticals is an API manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Its GMP standing is certified by EMA.

2
active US DMFs
0
valid CEPs
1
registered plants
7
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Xuzhou, China Not on file

What they file, and where

Molecule Regulators Docs
Febuxostat US FDA 1
Pitavastatin US FDA 1

Also appears on these molecule pages

Febuxostat API Pitavastatin API

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 7 None
EMA None 1

Questions about Wanbang Biopharmaceuticals

Does Wanbang Biopharmaceuticals hold a US DMF or a CEP?
Wanbang Biopharmaceuticals holds 2 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.
Where does Wanbang Biopharmaceuticals manufacture?
1 registered site is on record, in China (Xuzhou). Every site is listed on this page with the register it came from.
What does Wanbang Biopharmaceuticals make?
2 molecules are on record against Wanbang Biopharmaceuticals, including Febuxostat and Pitavastatin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Wanbang Biopharmaceuticals's GMP?
Current GMP certificates are on record from EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates