Naltrexone Hydrochloride 67046-0306
Product NDC
67046-0306- Manufacturer
- Coupler Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 15, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA090356
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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 (67046-0306-3)