NDC 85534-0036
Omeprazole 20 mg capsule, delayed release
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, 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
- Oct 31, 2014
- Package NDCs
85534-0036-085534-0036-185534-0036-285534-0036-3- Official label
- DailyMed (National Library of Medicine), updated Jul 13, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?