NDC 76519-1160
Naltrexone Hydrochloride 50 mg tablet, film coated
On the label: H.J. Harkins Co., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| H.J. Harkins Company, Inc. | Grover Beach, California, United States | Makes it, repackages it and relabels it | Problems found, fixed voluntarilyMar 3, 2023 · 5 inspections |
Product details
- Generic drug
- Naltrexone: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA075274
- On the market since
- Oct 17, 2017
- Package NDCs
76519-1160-5- Official label
- DailyMed (National Library of Medicine), updated Nov 29, 2017
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