Valsartan And Hydrochlorothiazide 65862-0549
Product NDC
65862-0549- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 21, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA202519
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Valsartan | 160 mg/1 |
Drug Class
Angiotensin 2 Receptor Blocker [EPC]Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]
Packaging Options(3)
10 BLISTER PACK in 1 CARTON (65862-549-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
90 TABLET, FILM COATED in 1 BOTTLE (65862-549-90)
1000 TABLET, FILM COATED in 1 BOTTLE (65862-549-99)