Dr. Reddy's Laboratories Limited
Medchal-Malkajgiri, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.
NDC 69181-158
Omeprazole 20 mg capsule, delayed release
On the label: Midwest Drug Distribution, Inc..
It's a repackaged product: Midwest Drug Distribution, Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-158.
Where the pills inside were made
Repackaging site
- Dr. Reddy's Laboratories Limited, Medchal-Malkajgiri, India · labels it
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA075576
- On the market since
- Feb 4, 2015
- Package NDCs
69181-158-14- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2015
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