NDC 70518-2251
Omeprazole 20 mg capsule, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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
- Aug 3, 2019
- Package NDCs
70518-2251-070518-2251-170518-2251-270518-2251-370518-2251-470518-2251-570518-2251-6- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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