NDC 70518-2226
Buprenorphine HCl 2 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0176.
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
- 2 mg
- Approval
- ANDA ANDA078633
- On the market since
- Jul 19, 2019
- Package NDCs
70518-2226-070518-2226-170518-2226-270518-2226-370518-2226-470518-2226-570518-2226-6- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2026
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