Valsartan And Hydrochlorothiazide 68180-0104
Product NDC
68180-0104- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 21, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA078946
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Valsartan | 160 mg/1 |
Drug Class
Angiotensin 2 Receptor Blocker [EPC]Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]