NDC 60290-102
Olmesartan Medoxomil and Hydrochlorothiazide 20 mg / 12.5 mg tablet
On the label: Umedica Laboratories USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA208847
- On the market since
- Feb 15, 2026
- Package NDCs
60290-102-0160290-102-0260290-102-0360290-102-0460290-102-05- Official label
- DailyMed (National Library of Medicine), updated Oct 23, 2026
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