NDC 70518-4198
Metoprolol Succinate 25 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-590.
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
- Apr 27, 2026 · Class II · Ascend Laboratories, LLC
Failed Dissolution Specifications
Lots: Lot # 25140859; Exp. Date: Jan 2027 - Jan 5, 2023 · Class II · Ascend Laboratories, LLC
Failed Dissolution Specification
Lots: Lot #s: 21143094, 21143095, 21143119, 21143121, 21142389, Exp 03/31/2023. - Jan 12, 2022 · Class II · Ascend Laboratories, LLC
Failed Dissolution Specifications.
Lots: Lot #: 21143093, Exp. March 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
- 25 mg
- Approval
- ANDA ANDA211143
- On the market since
- Oct 1, 2024
- Package NDCs
70518-4198-070518-4198-170518-4198-2- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
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