NDC 76420-055
Omeprazole 20 mg capsule, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, 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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, 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
- Oct 31, 2014
- Package NDCs
76420-055-0076420-055-0376420-055-0676420-055-0976420-055-1076420-055-12- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2025
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