Valsartan And Hydrochlorothiazide 71205-0042
Product NDC
71205-0042- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 20, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA201662
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Valsartan | 320 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Blocker [EPC]Angiotensin 2 Receptor Antagonists [MoA]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (71205-042-30)
60 TABLET, FILM COATED in 1 BOTTLE (71205-042-60)
90 TABLET, FILM COATED in 1 BOTTLE (71205-042-90)