NDC 64850-300
Naltrexone Hydrochloride 50 mg tablet, film coated
On the label: Elite Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Elite Laboratories, Inc. | Northvale, NJ, United States | Makes it and labels it | Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action |
Product details
- Generic drug
- Naltrexone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA075274
- On the market since
- Aug 15, 2025
- Package NDCs
64850-300-0164850-300-30- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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