NDC 62332-048
Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Alembic Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
| Alembic Pharmaceuticals Limited | Vadodara, India | Makes it | Problems found, fixed voluntarilyNov 22, 2024 · 1 inspection |
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg / 12.5 mg
- Approval
- ANDA ANDA091617
- On the market since
- May 23, 2016
- Package NDCs
62332-048-1062332-048-3062332-048-9062332-048-91- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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