Suppliers / Nantong Jinghua Pharmaceutical

Nantong Jinghua Pharmaceutical

China 46 employees Updated 9 July 2026

Nantong Jinghua Pharmaceutical is a contract manufacturer based in China. It holds 6 active US drug master files across a filed portfolio of 6 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 24 May 2024 as NAI.

6
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
3
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
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 24 May 2024 NAI US FDA
  • 29 April 2016 NAI US FDA
  • 12 July 2013 VAI US FDA
  • 11 March 2010 VAI US FDA

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

Registered plants

Site FDA FEI
China, China 3003735909

What they file, and where

Molecule Regulators Docs
Fluorouracil SFDA (Saudi Arabia), US FDA 2
Flucytosine US FDA 1
Indocyanine Green US FDA 1
Letermovir US FDA 1
Phenobarbital US FDA 1
Primidone US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None
US FDA None 1

Comparing suppliers?

Choose your molecules and target markets. Nantong Jinghua Pharmaceutical comes back tiered against every other supplier able to file there.

Start for free
No sales call.

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