| NDC Code | 0310-1087-95 |
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| Package Description | 7 TABLET, FILM COATED in 1 BOTTLE (0310-1087-95) |
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| Product NDC | 0310-1087 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dutoprol |
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| Non-Proprietary Name | Metoprolol Succinate And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20111230 |
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| End Marketing Date | 20170430 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021956 |
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| Manufacturer | AstraZeneca Pharmaceuticals LP |
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| Substance Name | METOPROLOL SUCCINATE; HYDROCHLOROTHIAZIDE |
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| Strength | 25; 12.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
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