NDC 70518-4570
buprenorphine hydrochloride 2 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Advagen Pharma Ltd.'s NDC 72888-182.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Rubicon Research Limited | Thane, India | Makes it, tests it, packages it and labels it | No problems foundMar 8, 2024 · 5 inspections |
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg
- Approval
- ANDA ANDA090279
- On the market since
- Feb 10, 2026
- Package NDCs
70518-4570-070518-4570-1- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2026
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