FDA NDC Directory · JSON-LD · Markdown

Sodium Chloride

NDC 76297-001 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerLABORATORIOS GRIFOLS SA
Marketing categoryAbbreviated NDA (generic) · App ANDA207956
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (9 g/1000mL)
Marketing started20170525
Package count9

External sources

Source: openFDA. Public-domain (CC0).