| NDC Code | 70934-705-90 |
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| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (70934-705-90) |
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| Product NDC | 70934-705 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
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| Non-Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20200513 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079106 |
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| Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
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| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
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| Strength | 5; 6.25 |
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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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