NDC 68071-4159
Losartan Potassium and Hydrochlorothiazide 100 mg / 12.5 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Alembic Pharmaceuticals Inc.'s NDC 62332-049.
Where the pills inside were 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 |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 100 mg / 12.5 mg
- Approval
- ANDA ANDA091617
- On the market since
- May 23, 2016
- Package NDCs
68071-4159-3- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2025
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