| NDC Code | 13668-325-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (13668-325-05) |
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| Product NDC | 13668-325 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20150603 |
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| End Marketing Date | 20200131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201593 |
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| Manufacturer | Torrent Pharmaceuticals Limited |
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| Substance Name | AMLODIPINE BESYLATE; VALSARTAN; HYDROCHLOROTHIAZIDE |
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| Strength | 10; 320; 25 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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