| NDC Code | 49884-174-11 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (49884-174-11) |
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| Product NDC | 49884-174 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine, Valsartan, Hydrochlorothiazide |
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| Non-Proprietary Name | Amlodipine Besylate Valsartan Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20150601 |
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| End Marketing Date | 20220531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201087 |
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| Manufacturer | Par Pharmaceutical, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN |
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| Strength | 10; 12.5; 160 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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