NDC 50228-342
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 20 mg / 12.5 mg tablet, film coated
On the label: ScieGen Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA208465
- On the market since
- May 19, 2026
- Package NDCs
50228-342-1050228-342-3050228-342-90- Official label
- DailyMed (National Library of Medicine), updated May 22, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?