Methadone Hydrochloride 81298-7500
Product NDC
81298-7500- Manufacturer
- Long Grove Pharmaceuticals, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 28, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA208306
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methadone Hydrochloride | 200 mg/20mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (81298-7500-1) / 20 mL in 1 VIAL, GLASS