| NDC Code | 57237-142-01 |
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| Package Description | 100 CAPSULE in 1 BOTTLE (57237-142-01) |
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| Product NDC | 57237-142 |
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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 | 20120905 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202239 |
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| Manufacturer | Rising Pharma Holdings, 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 | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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