| NDC Code | 0093-7038-56 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7038-56) |
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| Product NDC | 0093-7038 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine, Valsartan, And Hydrochlorothiazide |
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| Non-Proprietary Name | Amlodipine, 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 | 20141201 |
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| End Marketing Date | 20190228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200435 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; VALSARTAN; HYDROCHLOROTHIAZIDE |
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| Strength | 10; 160; 25 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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