NDC 67296-2123
Buprenorphine HCl 2 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. 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 |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg
- Approval
- ANDA ANDA078633
- On the market since
- Oct 8, 2009
- Package NDCs
67296-2123-3- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2025
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