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SODIUM CHLORIDE

NDC 0404-9978 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic namesodium chloride
Labeler / ManufacturerHenry Schein, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212248
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (4 meq/mL)
Marketing started20220112
Package count1

External sources

Source: openFDA. Public-domain (CC0).