| NDC Code | 0781-5952-37 |
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| Package Description | 3500 TABLET, FILM COATED in 1 BOTTLE (0781-5952-37) |
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| Product NDC | 0781-5952 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valsartan And Hydrochlorothiazide |
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| Non-Proprietary Name | Valsartan And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20120921 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020818 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | VALSARTAN; HYDROCHLOROTHIAZIDE |
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| Strength | 320; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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