Methadone Hydrochloride 00904-7417
Product NDC
00904-7417- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- January 3, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA088109
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methadone Hydrochloride | 10 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-7417-61) / 1 TABLET in 1 BLISTER PACK