Glenmark Pharmaceuticals Limited
Goa, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 7 inspections on record, 1 with serious problems.
NDC 71205-501
Omeprazole 10 mg capsule, delayed release
On the label: Proficient Rx LP.
It's a repackaged product: Proficient Rx LP rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-395.
Where the pills inside were made
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA091672
- On the market since
- Oct 31, 2014
- Package NDCs
71205-501-3071205-501-6071205-501-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?