NDC 72189-582
Buprenorphine Sublingual C-III 8 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx 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 |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 8 mg
- Approval
- ANDA ANDA078633
- On the market since
- Oct 15, 2024
- Package NDCs
72189-582-60- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2024
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