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Midazolam in Sodium Chloride

NDC 0143-9379 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216159
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsMIDAZOLAM HYDROCHLORIDE (1 mg/mL)
Marketing started20230519
Package count1

External sources

Source: openFDA. Public-domain (CC0).