High Outlier
DEA Schedule CIII
Strength
50 mg/mL
Manufacturer
Hospira Inc.NDC
00409205310
Classification
Generic
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAMUSCULAR; INTRAVENOUS
Last Updated
4/22/2026
Active Ingredients
KETAMINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA074549On Market Since
11/30/2004
Pharmacological Classes
General Anesthesia
General Anesthetic
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