NDC 70518-3389
Buprenorphine and Naloxone 2 mg / 8 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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
- Mar 16, 2022
- Package NDCs
70518-3389-0- Official label
- DailyMed (National Library of Medicine), updated May 22, 2026
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