NDC 70934-118
Omeprazole 20 mg capsule, delayed release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-158.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA075576
- On the market since
- May 11, 2018
- Package NDCs
70934-118-3070934-118-6070934-118-90- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?