NDC 53217-261
Naltrexone Hydrochloride 50 mg tablet, film coated
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC 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
- Strength
- 50 mg
- Approval
- ANDA ANDA075274
- On the market since
- Sep 23, 2013
- Package NDCs
53217-261-30- Official label
- DailyMed (National Library of Medicine), updated Mar 10, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?