Methohexital Sodium 23155-0893
Product NDC
23155-0893- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Injection
- Route
- Intramuscular, Intravenous, And Rectal
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 12, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA215488
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methohexital Sodium | 500 mg/500mg |
Drug Class
Barbiturate [EPC]Barbiturates [CS]
Packaging Options(1)
1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL