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Sodium Chloride

NDC 0409-6660 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic nameSODIUM CHLORIDE
Labeler / ManufacturerHospira, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018897
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (5.84 g/40mL)
Marketing started20050729
Package count1

External sources

Source: openFDA. Public-domain (CC0).