NDC 70518-2269
Olmesartan Medoxomil and Hydrochlorothiazide 40 mg / 12.5 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Alembic Pharmaceuticals Inc.'s NDC 62332-150.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, oral
- Strength
- 40 mg / 12.5 mg
- Approval
- ANDA ANDA204233
- On the market since
- Aug 16, 2019
- Package NDCs
70518-2269-0- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2026
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