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Midazolam In Sodium Chloride

NDC 68083-618 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218993
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMIDAZOLAM HYDROCHLORIDE (1 mg/mL)
Marketing started20240812
Package count1

External sources

Source: openFDA. Public-domain (CC0).