| NDC Code | 0023-5874-32 |
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| Package Description | 5 BOTTLE in 1 TRAY (0023-5874-32) > 30 TABLET, FILM COATED in 1 BOTTLE (0023-5874-31) |
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| Product NDC | 0023-5874 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Byvalson |
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| Non-Proprietary Name | Nebivolol Hydrochloride And Valsartan |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160603 |
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| Marketing Category Name | NDA |
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| Application Number | NDA206302 |
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| Manufacturer | Allergan, Inc. |
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| Substance Name | NEBIVOLOL HYDROCHLORIDE; VALSARTAN |
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| Strength | 5; 80 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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