FDA NDC Directory · JSON-LD · Markdown

Midazolam

NDC 76045-211 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMidazolam Hydrochloride
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203460
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMIDAZOLAM HYDROCHLORIDE (2 mg/2mL)
Marketing started20210416
Package count1

External sources

Source: openFDA. Public-domain (CC0).