Naltrexone Hydrochloride 70518-4344
Product NDC
70518-4344- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 20, 2025
- 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]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)