NDC 68071-2592
Buprenorphine 8 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-502.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Knoa Pharmaceuticals LLC | Wilson, NC, United States | Makes it | Problems found, fixed voluntarilySep 26, 2025 · 9 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 ANDA207276
- On the market since
- Oct 25, 2017
- Package NDCs
68071-2592-3- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2023
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