NDC 42708-199
Omeprazole 20 mg capsule, delayed release
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-161.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
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
- 20 mg
- Approval
- ANDA ANDA203270
- On the market since
- Aug 19, 2015
- Package NDCs
42708-199-14- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2026
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