Suppliers / Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd

Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd

China Updated 9 July 2026

Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd is an API manufacturer based in China. It appears in 36 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with NMPA (CN) and MINSA (CR).

0
active US DMFs
0
valid CEPs
0
registered plants
36
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Aztreonam SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Aztreonam API

Filings and GMP by regulator

Regulator Filings GMP certificates
NMPA (CN) 35 None
MINSA (CR) 1 None

Questions about Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd

Does Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd. It does have 36 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
What does Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd make?
1 molecule is on record against Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd, including Aztreonam. Each links through to that molecule's full manufacturer list.
Where does Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co.,Ltd file?
Filings are on record with NMPA (CN) and MINSA (CR), 36 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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Comparable suppliers

Apitoria Pharma shares 1 molecule Fresenius Kabi shares 1 molecule Guang'An Kingday Pharma And Chem shares 1 molecule Chongqing Shenghuaxi Pharmaceutical shares 1 molecule

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