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Sodium Chloride

NDC 0487-4301 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerNephron Pharmaceuticals Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA211968
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (9 mg/mL)
Marketing started20200604
Package count4

External sources

Source: openFDA. Public-domain (CC0).