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Sodium Nitroprusside

NDC 75907-290 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerDr.Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA210114
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM NITROPRUSSIDE (50 mg/2mL)
Marketing started20251201
Package count1

External sources

Source: openFDA. Public-domain (CC0).