Ketamine Hydrochloride 00404-9882
Product NDC
00404-9882- Manufacturer
- Henry Schein, Inc.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- January 11, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA074549
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ketamine Hydrochloride | 50 mg/mL |
Drug Class
General Anesthesia [PE]General Anesthetic [EPC]
Packaging Options(1)
1 VIAL in 1 BAG (0404-9882-10) / 10 mL in 1 VIAL