| NDC Code | 21695-809-30 |
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| Package Description | 30 TABLET, COATED in 1 BOTTLE (21695-809-30) |
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| Product NDC | 21695-809 |
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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, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20000925 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075579 |
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| Manufacturer | Rebel Distributors Corp |
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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],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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