NDC 67296-2164
Buprenorphine and Naloxone 2 mg / 8 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-602.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Halo Pharmaceutical Inc | Whippany, NJ, United States | Makes it | No problems foundDec 8, 2025 · 13 inspections |
| Knoa Pharmaceuticals LLC | Wilson, NC, United States | Makes it | Problems found, fixed voluntarilySep 26, 2025 · 9 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg / 8 mg
- Approval
- ANDA ANDA205601
- On the market since
- Apr 13, 2020
- Package NDCs
67296-2164-167296-2164-6- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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