FDA NDC Directory · JSON-LD · Markdown

0.9% SODIUM CHLORIDE

NDC 51662-1609 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA207956
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (9 g/1000mL)
Marketing started20220731
Package count1

External sources

Source: openFDA. Public-domain (CC0).