Losartan Potassium And Hydrochlorothiazide 68071-4159
Product NDC
68071-4159- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 23, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA091617
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Losartan Potassium | 100 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (68071-4159-3)