Naltrexone Hydrochloride 00406-1170
Product NDC
00406-1170- Manufacturer
- Specgx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 22, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA076264
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naltrexone Hydrochloride | 50 mg/1 |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)
30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)