Dr. Reddy's Laboratories Limited
Medchal-Malkajgiri, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.
NDC 70934-113
Metoprolol succinate 25 mg tablet, extended release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals..
It's a repackaged product: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-466.
Where the pills inside were made
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, · repackages it
Recalls
- May 23, 2014 · Class II · Terminated
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 · Terminated
Failed Dissolution Specification; 12-Month stability interval.
Lots: Lot # C207420 and C207416
Product details
- Generic drug
- Metoprolol: see every company that makes it
- Form
- tablet, extended release
- Strength
- 25 mg
- Approval
- ANDA ANDA090617
- On the market since
- May 9, 2018
- Package NDCs
70934-113-30- Official label
- DailyMed (National Library of Medicine), updated Jun 18, 2018
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