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Sodium Chloride

NDC 46163-300 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Medical Care de Mexico, S.A. de C.V.
Marketing categoryAbbreviated NDA (generic) · App ANDA078177
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (900 mg/100mL)
Marketing started20070412
Package count1

External sources

Source: openFDA. Public-domain (CC0).