NDC 42708-162
Atenolol 50 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-169.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it and tests it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Atenolol: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA078512
- On the market since
- Oct 31, 2007
- Package NDCs
42708-162-30- Official label
- DailyMed (National Library of Medicine), updated Dec 3, 2025
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