FDA NDC Directory · JSON-LD · Markdown

SODIUM NITROPRUSSIDE

NDC 55150-320 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAuroMedics Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211934
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM NITROPRUSSIDE (50 mg/2mL)
Marketing started20201210
Package count1

External sources

Source: openFDA. Public-domain (CC0).