NDC 31722-887
Olmesartan medoxomil and hydrochlorothiazide 40 mg / 12.5 mg tablet, film coated
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 40 mg / 12.5 mg
- Approval
- ANDA ANDA209199
- On the market since
- Jul 25, 2025
- Package NDCs
31722-887-3031722-887-3231722-887-90- Official label
- DailyMed (National Library of Medicine), updated Aug 26, 2025
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