Suppliers / Shaoxing Jingxin Pharmaceutical

Shaoxing Jingxin Pharmaceutical

China Updated 9 July 2026

Shaoxing Jingxin Pharmaceutical is an API manufacturer based in China. It holds 7 active US drug master files and 12 valid CEPs across a filed portfolio of 9 molecules. Its GMP standing is certified by MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 24 May 2024 as NAI.

7
active US DMFs
12
valid CEPs
2
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
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 24 May 2024 NAI US FDA

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

Registered plants

Site FDA FEI
Shangyu, China Not on file
China, China 3006305239

What they file, and where

Molecule Regulators Docs
Rosuvastatin EDQM, US FDA 5
Levetiracetam EDQM, US FDA 3
Simvastatin EDQM 3
Rivaroxaban EDQM, US FDA 2
Ticagrelor EDQM, US FDA 2
Apixaban US FDA 1
Brivaracetam US FDA 1
Enrofloxacin For Veterinary Use EDQM 1
Levofloxacin EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MFDS (Korea) None 2
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was NAI, on 24 May 2024.

Sources on this page

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