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 50436-8158
Omeprazole 20 mg capsule, delayed release
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-158.
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 ANDA075576
- On the market since
- Jan 21, 2009
- Package NDCs
50436-8158-150436-8158-2- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?