Methadone Hydrochloride 00054-0709
Product NDC
00054-0709- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- March 8, 1983
- Listing Expires
- December 31, 2027
- Application
- ANDA088109
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methadone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
1 BLISTER PACK in 1 CARTON (0054-0709-20) / 100 TABLET in 1 BLISTER PACK
100 TABLET in 1 BOTTLE, PLASTIC (0054-0709-25)