NDC 31722-482
Buprenorphine and Naloxone 3 mg / 12 mg film, soluble
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- film, soluble, buccal; sublingual
- Strength
- 3 mg / 12 mg
- Approval
- ANDA ANDA219850
- On the market since
- May 1, 2026
- Package NDCs
31722-482-3031722-482-31- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2026
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