| NDC Code | 58118-2279-0 |
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| Package Description | 1 CAPSULE in 1 PACKET (58118-2279-0) |
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| Product NDC | 58118-2279 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine Besylate And Benazepril Hydrochloride |
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| Non-Proprietary Name | Amlodipine Besylate And Benazepril Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 19950303 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020364 |
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| Manufacturer | Clinical Solutions Wholesale |
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| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
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| Strength | 10; 40 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
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