Amlodipine, Valsartan And Hydrochlorothiazide 65862-0834
Product NDC
65862-0834- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 19, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA206180
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 5 mg/1 |
| Hydrochlorothiazide | 12.5 mg/1 |
| Valsartan | 160 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Blocker [EPC]Angiotensin 2 Receptor Antagonists [MoA]
Packaging Options(3)
500 TABLET, FILM COATED in 1 BOTTLE (65862-834-05)
30 TABLET, FILM COATED in 1 BOTTLE (65862-834-30)
90 TABLET, FILM COATED in 1 BOTTLE (65862-834-90)