| NDC Code | 16714-417-03 |
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| Package Description | 1000 TABLET in 1 BOTTLE (16714-417-03) |
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| Product NDC | 16714-417 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
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| Proprietary Name Suffix | 50 Mg-25 Mg |
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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 | 20130917 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202870 |
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| Manufacturer | NorthStar RxLLC |
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| Substance Name | METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE |
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| Strength | 50; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
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