| NDC Code | 70771-1188-0 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1188-0) |
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| Product NDC | 70771-1188 |
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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 | 20180104 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207771 |
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| Manufacturer | Zydus Lifesciences Limited |
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| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
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| Strength | 5; 40 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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