Naltrexone Hydrochloride 71335-2062
Product NDC
71335-2062- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 29, 2012
- Listing Expires
- December 31, 2026
- 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(6)
30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)
45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)
120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)
15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)