Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg / 0.5 mg
- Approval
- ANDA ANDA205022
- On the market since
- Sep 19, 2016
- Package NDCs
62175-452-32- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2026
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