Losartan Potassium And Hydrochlorothiazide 16714-0226
Product NDC
16714-0226- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 4, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA091629
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Losartan Potassium | 50 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (16714-226-01)
90 TABLET, FILM COATED in 1 BOTTLE (16714-226-02)
1000 TABLET, FILM COATED in 1 BOTTLE (16714-226-04)