DEA Schedule CIII
Strength
50 mg/mL
Manufacturer
Hikma Pharmaceuticals USA Inc.NDC
00143950810
Classification
Generic
Dosage Form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS
Last Updated
4/22/2026
Active Ingredients
KETAMINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA074524On Market Since
7/1/1996
Pharmacological Classes
General Anesthesia
General Anesthetic
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