Glenmark Pharmaceuticals Limited
Goa, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 7 inspections on record, 1 with serious problems.
NDC 50436-0396
Omeprazole 20 mg capsule, delayed release
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-396.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA091672
- On the market since
- Oct 31, 2014
- Package NDCs
50436-0396-150436-0396-250436-0396-3- Official label
- DailyMed (National Library of Medicine), updated May 8, 2019
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