NDC 70518-4754
Olmesartan medoxomil and hydrochlorothiazide 40 mg / 12.5 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-887.
Where the pills inside were 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
- Sep 15, 2026
- Package NDCs
70518-4754-0- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2026
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