NDC 70518-2014
Buprenorphine HCl 8 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0177.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 8 mg
- Approval
- ANDA ANDA078633
- On the market since
- Apr 12, 2019
- Package NDCs
70518-2014-070518-2014-170518-2014-270518-2014-3- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2026
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