Ketamine Hydrochloride 00409-2051
Product NDC
00409-2051- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- November 30, 2004
- Listing Expires
- December 31, 2027
- Application
- ANDA074549
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ketamine Hydrochloride | 100 mg/mL |
Drug Class
General Anesthesia [PE]General Anesthetic [EPC]
Packaging Options(1)
10 VIAL, MULTI-DOSE in 1 BOX (0409-2051-05) / 5 mL in 1 VIAL, MULTI-DOSE (0409-2051-15)