Naltrexone Hydrochloride 71335-0014
Product NDC
71335-0014- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 18, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA091205
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naltrexone Hydrochloride | 50 mg/1 |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(7)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0014-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0014-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0014-3)
45 TABLET, FILM COATED in 1 BOTTLE (71335-0014-4)
120 TABLET, FILM COATED in 1 BOTTLE (71335-0014-5)
15 TABLET, FILM COATED in 1 BOTTLE (71335-0014-6)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0014-7)