NDC 23155-886
Naltrexone Hydrochloride 50 mg tablet, film coated
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Chartwell Pharmaceuticals Congers, LLC. | Congers, NY, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionNov 18, 2025 · 8 inspections, 2 with FDA action |
Product details
- Generic drug
- Naltrexone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA207905
- On the market since
- Oct 6, 2023
- Package NDCs
23155-886-0123155-886-03- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2025
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