NDC 68071-2199
Omeprazole 40 mg capsule, delayed release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-397.
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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA091672
- On the market since
- Oct 31, 2014
- Package NDCs
68071-2199-468071-2199-668071-2199-768071-2199-9- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
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