| NDC Code | 57664-799-83 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-799-83) |
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| Product NDC | 57664-799 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide |
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| Non-Proprietary Name | Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20161026 |
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| End Marketing Date | 20240630 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA200175 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
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| Strength | 5; 25; 40 |
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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], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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