Methadone Hydrochloride 51991-0002
Product NDC
51991-0002- Manufacturer
- Breckenridge Pharmaceutical Inc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- December 30, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218252
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methadone Hydrochloride | 10 mg/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (51991-002-98) / 20 mL in 1 VIAL, GLASS