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ketamine hydrochloride

NDC 65219-184 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215808
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsKETAMINE HYDROCHLORIDE (10 mg/mL)
Marketing started20230710
Package count1

External sources

Source: openFDA. Public-domain (CC0).