Naltrexone Hydrochloride 68071-3654-03
- Manufacturer
- Nucare Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 15, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA075274
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naltrexone Hydrochloride | 50 mg/1 |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Selected Package
68071-3654-03Selected30 TABLET, FILM COATED in 1 BOTTLE (68071-3654-3)