Naltrexone Hydrochloride 47335-0326-88
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- 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]
Selected Package
47335-0326-88Selected100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88)
Other packages for this product(3)
100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
30 TABLET, FILM COATED in 1 BOTTLE (47335-326-83)