Suppliers / Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical

Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical

China Updated 9 July 2026

Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical is an API and finished-dose manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 3 molecules. Its filings concentrate with MINSA (CR) and ARCSA (EC).

2
active US DMFs
0
valid CEPs
0
registered plants
4
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Cefsulodin US FDA 1
Gentamicin SFDA (Saudi Arabia) 1
Tigecycline US FDA 1

Also appears on these molecule pages

Aztreonam finished dose Gentamicin API Tigecycline API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None
ARCSA (EC) 1 None

Questions about Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical

Does Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical hold a US DMF or a CEP?
Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical 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.
What does Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical make?
3 molecules are on record against Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical, including Cefsulodin, Gentamicin and Tigecycline. Each links through to that molecule's full manufacturer list.
Where does Fuan Pharmaceutical Group Yantai Justaware Pharmaceutical file?
Filings are on record with MINSA (CR) and ARCSA (EC), 4 in total.

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