| NDC Code | 0093-7370-01 |
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| Package Description | 100 CAPSULE in 1 BOTTLE (0093-7370-01) |
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| Product NDC | 0093-7370 |
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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 | 20070518 |
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| End Marketing Date | 20200229 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077179 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
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| Strength | 2.5; 10 |
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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 [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
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