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Sodium chloride

NDC 65219-232 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameSODIUM CHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208122
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (2250 mg/500mL)
Marketing started20180723
Package count1

External sources

Source: openFDA. Public-domain (CC0).