NDC 67046-1109
Metoprolol Succinate 100 mg tablet, film coated, extended release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-502.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Recalls
- Jan 11, 2023 · Class II · Amerisource Health Services LLC
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Lots: Lots: (a) 21143211, EXP 03/31/2023; (b) 21143185, 21143193, EXP 02/28/2023 - Dec 20, 2021 · Class II · American Health Packaging
Failed Dissolution Specifications
Lots: Lots# 21141983, 21141984 and 21141985, Exp 03/31/2023; Lots# 21142017, 21142018, 21142019, Exp 02/28/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Metoprolol: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 100 mg
- Approval
- ANDA ANDA211143
- On the market since
- Nov 12, 2024
- Package NDCs
67046-1109-3- Official label
- DailyMed (National Library of Medicine), updated Nov 12, 2024
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