Aurobindo Pharma Limited
Medchal, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.
NDC 42708-147
Metoprolol Tartrate 50 mg tablet, film coated
On the label: QPharma, Inc..
It's a repackaged product: QPharma, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-101.
Where the pills inside were made
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Metoprolol: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA077739
- On the market since
- Sep 11, 2007
- Package NDCs
42708-147-60- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2025
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