FDA NDC Directory · JSON-LD · Markdown

SODIUM CHLORIDE

NDC 51662-1522 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA016366
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (900 mg/100mL)
Marketing started20200804
Package count1

External sources

Source: openFDA. Public-domain (CC0).