NDC 70518-4517
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 Macleods Pharmaceuticals Limited's NDC 33342-174.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | Daman, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 26, 2023 · 4 inspections |
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 ANDA204801
- On the market since
- Nov 10, 2025
- Package NDCs
70518-4517-0- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2026
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