FDA NDC Directory · JSON-LD · Markdown

Sodium Chloride

NDC 63323-530 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209476
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (3 g/100mL)
Marketing started20200320
Package count1

External sources

Source: openFDA. Public-domain (CC0).