NDC 87441-063
Omeprazole 20 mg capsule, delayed release
On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-396.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- Unit Dose Solutions, Inc., Raleigh, NC, United States · repackages it
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA091672
- On the market since
- Jun 30, 2026
- Package NDCs
87441-063-01- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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