NDC 71335-3104 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-3104
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
- September 23, 2013
- Marketing end
- November 30, 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 |
|---|---|---|
| 71335-3104-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-3104-1) | Mar 16, 2026 |
| 71335-3104-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-3104-2) | Mar 16, 2026 |
| 71335-3104-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-3104-3) | Mar 16, 2026 |
| 71335-3104-4 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-3104-4) | Mar 16, 2026 |
| 71335-3104-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-3104-5) | Mar 16, 2026 |
| 71335-3104-6 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-3104-6) | Mar 16, 2026 |
| 71335-3104-7 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3104-7) | Mar 16, 2026 |
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