NDC 70518-4344
Naltrexone Hydrochloride 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from TAGI Pharma, Inc.'s NDC 51224-206.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Elite Laboratories, Inc. | Northvale, NJ, United States | Makes 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
- May 20, 2025
- Package NDCs
70518-4344-0- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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