Amlodipine Valsartan And Hydrochlorothiazide 00078-1280
Product NDC
00078-1280- Manufacturer
- Novartis Pharmaceuticals Corporation
- Dosage Form
- Tablet, Film Coated
- Product Type
- Human Prescription Drug
- Marketing Start
- April 4, 2009
- Listing Expires
- December 31, 2027
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 10 mg/1 |
| Hydrochlorothiazide | 25 mg/1 |
| Valsartan | 320 mg/1 |
Packaging Options(1)
25000 TABLET, FILM COATED in 1 DRUM (0078-1280-01)