Losartan Potassium And Hydrochlorothiazide 59746-0339
Product NDC
59746-0339- Manufacturer
- Jubilant Cadista Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 30, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA201845
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Losartan Potassium | 100 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (59746-339-01)
1000 TABLET, FILM COATED in 1 BOTTLE (59746-339-10)
30 TABLET, FILM COATED in 1 BOTTLE (59746-339-30)
90 TABLET, FILM COATED in 1 BOTTLE (59746-339-90)