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Ketamine Hydrochloride

NDC 0143-9508 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074524
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsKETAMINE HYDROCHLORIDE (50 mg/mL)
Marketing started19960701
Package count1

External sources

Source: openFDA. Public-domain (CC0).