Losartan Potassium And Hydrochlorothiazide 00093-7367
Product NDC
00093-7367- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 6, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA077157
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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)
1000 TABLET, FILM COATED in 1 BOTTLE (0093-7367-10)
30 TABLET, FILM COATED in 1 BOTTLE (0093-7367-56)
90 TABLET, FILM COATED in 1 BOTTLE (0093-7367-98)