| NDC Code | 49884-664-09 |
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| Package Description | 90 TABLET in 1 BOTTLE (49884-664-09) |
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| Product NDC | 49884-664 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Candesartan Cilexetil-hydrochlorothiazide |
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| Non-Proprietary Name | Candesartan Cilexetil Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20121205 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021093 |
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| Manufacturer | Par Pharmaceutical Inc. |
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| Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
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| Strength | 32; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
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