| NDC Code | 68071-1882-3 |
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| Package Description | 30 TABLET in 1 BOTTLE (68071-1882-3) |
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| Product NDC | 68071-1882 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20130419 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203145 |
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| Manufacturer | NuCare Pharmaceuticals, Inc. |
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| Substance Name | VALSARTAN; HYDROCHLOROTHIAZIDE |
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| Strength | 160; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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