NDC 16714-226
Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Northstar Rx LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
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 ANDA091629
- On the market since
- Sep 4, 2024
- Package NDCs
16714-226-0116714-226-0216714-226-04- Official label
- DailyMed (National Library of Medicine), updated Sep 6, 2025
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