NDC 0904-6917
Omeprazole 20 mg capsule, delayed release
On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-412.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA091352
- On the market since
- Nov 23, 2012
- Package NDCs
0904-6917-61- Official label
- DailyMed (National Library of Medicine), updated Sep 19, 2025
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