NDC 70518-3680
Metoprolol Succinate 50 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-591.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
Recalls
- Jan 5, 2023 · Class II · Ascend Laboratories, LLC
Failed Dissolution Specification
Lots: Lot #: 21142633, Exp 03/31/2023 - Jan 5, 2023 · Class II · Ascend Laboratories, LLC
Failed Dissolution Specification
Lots: Lot#: 21141321, 21141322, Exp 01/31/2023.
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, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA211143
- On the market since
- Mar 13, 2023
- Package NDCs
70518-3680-070518-3680-1- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
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