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 70518-0199
Omeprazole 40 mg capsule, delayed release
On the label: Remedyrepack Inc..
It's a repackaged product: Remedyrepack Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-397.
Where the pills inside were made
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA091672
- On the market since
- Feb 6, 2017
- Package NDCs
70518-0199-070518-0199-170518-0199-270518-0199-370518-0199-4- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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