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Enalaprilat

NDC 0143-9787 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameenalaprilat
Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078687
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsENALAPRILAT DIHYDRATE (1.25 mg/mL)
Marketing started20081223
Package count1

External sources

Source: openFDA. Public-domain (CC0).