Naltrexone Hydrochloride 62135-0242
Product NDC
62135-0242- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 21, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207905
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naltrexone Hydrochloride | 50 mg/1 |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (62135-242-30)
60 TABLET, FILM COATED in 1 BOTTLE (62135-242-60)
90 TABLET, FILM COATED in 1 BOTTLE (62135-242-90)