NDC 42291-632 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC42291-632
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- AvKARE
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075274
- Marketed since
- March 26, 2015
- Marketing end
- June 30, 2028
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naltrexone Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Naltrexone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 42291-632-30 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30) | Mar 26, 2015 |
| 42291-632-60 | 60 TABLET, FILM COATED in 1 BOTTLE (42291-632-60) | Jul 24, 2025 |
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