FDA NDC Directory · JSON-LD · Markdown

Midazolam In Sodium Chloride

NDC 65219-650 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFRESENIUS KABI USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218993
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMIDAZOLAM HYDROCHLORIDE (1 mg/mL)
Marketing started20250115
Package count2

External sources

Source: openFDA. Public-domain (CC0).