| NDC Code | 68084-726-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-726-32) > 1 CAPSULE in 1 BLISTER PACK (68084-726-33) |
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| Product NDC | 68084-726 |
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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 | 20140602 |
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| End Marketing Date | 20170531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077183 |
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| Manufacturer | American Health Packaging |
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| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
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| Strength | 10; 20 |
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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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