NDC 67296-2228
Buprenorphine and Naloxone 2 mg / 0.5 mg film
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Ingenus Pharmaceuticals, LLC's NDC 50742-397.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aveva Drug Delivery Systems Inc. | Miramar, FL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 14, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- film, buccal; sublingual
- Strength
- 2 mg / 0.5 mg
- Approval
- ANDA ANDA212756
- On the market since
- Aug 29, 2023
- Package NDCs
67296-2228-167296-2228-3- Official label
- DailyMed (National Library of Medicine), updated Apr 22, 2026
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