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SODIUM NITROPRUSSIDE

NDC 42571-265 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209352
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM NITROPRUSSIDE (50 mg/2mL)
Marketing started20171230
Package count1

External sources

Source: openFDA. Public-domain (CC0).