| NDC Code | 59212-095-30 |
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| Package Description | 30 TABLET in 1 BOTTLE (59212-095-30) |
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| Product NDC | 59212-095 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20140701 |
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| End Marketing Date | 20220930 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021956 |
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| Manufacturer | Concordia Pharmaceuticals Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE |
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| Strength | 12.5; 50 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |
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