FDA NDC Directory · JSON-LD · Markdown

Sodium Chloride

NDC 63323-186 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameSODIUM CHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA088912
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (9 mg/mL)
Marketing started20000810
Package count3

External sources

Source: openFDA. Public-domain (CC0).