NDC 55154-7280
Metoprolol succinate 25 mg tablet, film coated, extended release
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-466.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Recalls
- May 23, 2014 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.
Lots: Lot # C206578 Exp. 05/2014 Lot # C207415 Exp. 06/2014 - Dec 13, 2013 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specification; 12-Month stability interval.
Lots: Lot # C207420 and C207416
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 ANDA090617
- On the market since
- Sep 10, 2012
- Package NDCs
55154-7280-0- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2025
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