| NDC Code | 70771-1762-3 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1762-3) |
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| Product NDC | 70771-1762 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20230301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215666 |
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| Manufacturer | Zydus Lifesciences Limited |
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| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
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| Strength | 10; 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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