NDC 65862-779
Olmesartan Medoxomil and Hydrochlorothiazide 20 mg / 12.5 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA205391
- On the market since
- Apr 24, 2017
- Package NDCs
65862-779-1065862-779-3065862-779-7865862-779-9065862-779-99- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2025
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