NDC 67877-453
Olmesartan Medoxomil And Hydrochlorothiazide 20 mg / 12.5 mg tablet, film coated
On the label: Ascend Laboratories, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
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 ANDA207037
- On the market since
- May 1, 2025
- Package NDCs
67877-453-3067877-453-90- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2026
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