NDC 42708-158
Omeprazole 10 mg capsule, delayed release
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-157.
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 |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA075576
- On the market since
- Jan 21, 2009
- Package NDCs
42708-158-14- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2025
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