NDC 85509-1396
Omeprazole 20 mg capsule, delayed release
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC 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
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels 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
- Jan 20, 2017
- Package NDCs
85509-1396-185509-1396-285509-1396-385509-1396-685509-1396-9- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2025
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