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Sodium Chloride

NDC 0641-6144 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201833
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsSODIUM CHLORIDE (9 mg/mL)
Marketing started20130924
Package count1

External sources

Source: openFDA. Public-domain (CC0).