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 70934-773
Omeprazole 10 mg capsule, delayed release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals..
It's a repackaged product: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-157.
Where the pills inside were made
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, · repackages it
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release
- Strength
- 10 mg
- Approval
- ANDA ANDA075576
- On the market since
- Jun 8, 2020
- Package NDCs
70934-773-90- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2020
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