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.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| China, China | 3003735909 |
| 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
| Regulator | Filings | GMP certificates |
|---|---|---|
| MINSA (CR) | 3 | None |
| US FDA | None | 1 |
Choose your molecules and target markets. Nantong Jinghua Pharmaceutical comes back tiered against every other supplier able to file there.
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