| NDC Code | 0781-5631-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (0781-5631-01) |
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| Product NDC | 0781-5631 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
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| Non-Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19841201 |
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| End Marketing Date | 20140430 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA018303 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
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| Strength | 25; 100 |
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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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