NDC 60687-481
Buprenorphine 2 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-501.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Knoa Pharmaceuticals LLC | Wilson, NC, United States | Makes it | Problems found, fixed voluntarilySep 26, 2025 · 9 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Aug 19, 2026 · Class III · American Health Packaging
Labeling: Label Mix-up
Lots: Lot # 1030023, Exp Date: 06/30/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg
- Approval
- ANDA ANDA207276
- On the market since
- Feb 6, 2020
- Package NDCs
60687-481-1160687-481-21- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?