| NDC Code | 0591-3759-01 |
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| Package Description | 100 CAPSULE in 1 BOTTLE (0591-3759-01) |
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| Product NDC | 0591-3759 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine And Benazepril Hydrochloride |
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| Non-Proprietary Name | Amlodipine And Benazepril Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20101015 |
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| End Marketing Date | 20190831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077890 |
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| Manufacturer | Actavis Pharma, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
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| Strength | 5; 20 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |
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