NDC 71335-2419 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2419
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075274
- Marketed since
- February 15, 2024
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 71335-2419-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2419-1) | Nov 12, 2024 |
| 71335-2419-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2419-2) | Nov 12, 2024 |
| 71335-2419-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2419-3) | Nov 12, 2024 |
| 71335-2419-4 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-2419-4) | Nov 12, 2024 |
| 71335-2419-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2419-5) | Nov 12, 2024 |
| 71335-2419-6 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2419-6) | Nov 12, 2024 |
| 71335-2419-7 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2419-7) | Nov 12, 2024 |
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