| NDC Code | 60505-4582-3 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4582-3) |
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| Product NDC | 60505-4582 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine And Olmesartan Medoxomil |
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| Non-Proprietary Name | Amlodipine And Olmesartan Medoxomil |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20170815 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207807 |
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| Manufacturer | Apotex Corp. |
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| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
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| Strength | 5; 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 [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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