Losartan Potassium And Hydrochlorothiazide 71335-0152
Product NDC
71335-0152- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 6, 2010
- 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(8)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3)
120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)
58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6)
180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7)
1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)