| NDC Code | 0378-1722-05 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1722-05) |
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| Product NDC | 0378-1722 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine Besylate And Valsartan |
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| Non-Proprietary Name | Amlodipine Besylate And Valsartan |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20150330 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090483 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | AMLODIPINE BESYLATE; VALSARTAN |
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| Strength | 10; 160 |
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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 [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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