Suppliers / Livzon Group Fuzhou Fuxing Pharmaceutical

Livzon Group Fuzhou Fuxing Pharmaceutical

China 16 employees Updated 9 July 2026

Livzon Group Fuzhou Fuxing Pharmaceutical is an API manufacturer based in China. It holds 15 active US drug master files and 14 valid CEPs across a filed portfolio of 17 molecules. Its GMP standing is certified by US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 5 April 2024 as NAI.

15
active US DMFs
14
valid CEPs
4
registered plants 1 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 5 April 2024 NAI US FDA
  • 3 August 2018 VAI US FDA
  • 20 March 2015 NAI US FDA
  • 11 November 2011 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Fuzhou, China Not on file
Jiangyin, China Not on file
Fujian, China Not on file
China, China 3006772356

What they file, and where

Molecule Regulators Docs
Colistimethate EDQM, SFDA (Saudi Arabia), US FDA 4
Tobramycin EDQM, US FDA 4
Vancomycin SFDA (Saudi Arabia), US FDA 4
Daptomycin SFDA (Saudi Arabia), US FDA 3
Teicoplanin EDQM, SFDA (Saudi Arabia) 3
Vancomycin Hydrochloride EDQM 3
Acarbose EDQM, US FDA 2
Milbemycin Oxime For Veterinary Use EDQM 2
Polymyxin B EDQM, US FDA 2
Colistin EDQM 1
Show all 17 molecules on file
Dalbavancin US FDA 1
Gentamicin US FDA 1
Kanamycin US FDA 1
Moxidectin US FDA 1
Moxidectin For Veterinary Use EDQM 1
Sirolimus US FDA 1
Telavancin US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
US FDA None 1
EMA None 1

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Open risk flags

  • The most recent inspection outcome was NAI, on 5 April 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates