| NDC Code | 0115-5322-02 |
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| Package Description | 500 TABLET in 1 BOTTLE (0115-5322-02) |
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| Product NDC | 0115-5322 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nadolol And Bendroflumethiazide |
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| Non-Proprietary Name | Nadolol And Bendroflumethiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20070330 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077833 |
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| Manufacturer | Impax Generics |
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| Substance Name | NADOLOL; BENDROFLUMETHIAZIDE |
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| Strength | 80; 5 |
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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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