NDC 71335-2062 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2062
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090356
- Marketed since
- February 29, 2012
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2062-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1) | Mar 21, 2022 |
| 71335-2062-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2) | Mar 21, 2022 |
| 71335-2062-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3) | Mar 21, 2022 |
| 71335-2062-4 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4) | Mar 21, 2022 |
| 71335-2062-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5) | Mar 21, 2022 |
| 71335-2062-6 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6) | Mar 21, 2022 |
| 71335-2062-7 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2062-7) | Mar 21, 2022 |
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