NDC 62135-242 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC62135-242
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207905
- Marketed since
- July 21, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naltrexone Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Naltrexone Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62135-242-30 | 30 TABLET, FILM COATED in 1 BOTTLE (62135-242-30) | Jan 5, 2022 |
| 62135-242-60 | 60 TABLET, FILM COATED in 1 BOTTLE (62135-242-60) | Jun 11, 2024 |
| 62135-242-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-242-90) | Jan 5, 2022 |
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