FDA NDC Directory · JSON-LD · Markdown

NIPRIDE RTU

NDC 51754-1029 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameSodium Nitroprusside
Labeler / ManufacturerEXELA PHARMA SCIENCES, LLC
Marketing categoryNew Drug Application (innovator) · App NDA209387
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM NITROPRUSSIDE (.2 mg/mL)
Marketing started20180720
Package count1

External sources

Source: openFDA. Public-domain (CC0).