NDC 70518-4577
Olmesartan Medoxomil And Hydrochlorothiazide 25 mg / 40 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-451.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg / 40 mg
- Approval
- ANDA ANDA207037
- On the market since
- Feb 27, 2026
- Package NDCs
70518-4577-0- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?