| NDC Code | 0186-0322-54 |
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| Package Description | 90 TABLET in 1 BOTTLE (0186-0322-54) |
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| Product NDC | 0186-0322 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atacand Hct |
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| Non-Proprietary Name | Candesartan Cilexetil And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20000928 |
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| End Marketing Date | 20201231 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021093 |
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| Manufacturer | AstraZeneca Pharmaceuticals LP |
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| Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
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| Strength | 32; 12.5 |
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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 [CS] |
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