FDA NDC Directory · JSON-LD · Markdown

Sodium nitroprusside

NDC 70121-1189 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209493
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM NITROPRUSSIDE (25 mg/mL)
Marketing started20171107
Package count1

External sources

Source: openFDA. Public-domain (CC0).