NDC 68071-2915
Buprenorphine HCl 8 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.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 |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet
- Strength
- 8 mg
- Approval
- ANDA ANDA078633
- On the market since
- Oct 8, 2009
- Package NDCs
68071-2915-3- Official label
- DailyMed (National Library of Medicine), updated Jan 17, 2023
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