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 72789-482
Omeprazole 20 mg capsule, delayed release
On the label: PD-Rx Pharmaceuticals, Inc..
It's a repackaged product: PD-Rx Pharmaceuticals, Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-644.
Where the pills inside were made
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078490
- On the market since
- Mar 1, 2014
- Package NDCs
72789-482-1472789-482-3072789-482-6072789-482-90- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?