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Ketamine Hydrochloride

NDC 25021-684 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA216809
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsKETAMINE HYDROCHLORIDE (100 mg/mL)
Marketing started20230715
Package count1

External sources

Source: openFDA. Public-domain (CC0).