| NDC Code | 68788-6880-2 |
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| Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (68788-6880-2) |
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| Product NDC | 68788-6880 |
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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 | 20170123 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079106 |
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| Manufacturer | Preferred Pharmaceuticals Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE |
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| Strength | 6.25; 5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
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