NDC 42571-245
OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE 5 mg / 20 mg / 12.5 mg tablet, film coated
On the label: Micro Labs Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Micro Labs Limited | Verna, India | Makes it | Problems found, fixed voluntarilyMay 30, 2025 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Amlodipine and Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg / 20 mg / 12.5 mg
- Approval
- ANDA ANDA207437
- On the market since
- Mar 1, 2026
- Package NDCs
42571-245-0542571-245-1042571-245-3042571-245-90- Official label
- DailyMed (National Library of Medicine), updated Nov 29, 2025
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