| NDC Code | 68382-434-16 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68382-434-16) |
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| Product NDC | 68382-434 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine And Atorvastatin |
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| Non-Proprietary Name | Amlodipine And Atorvastatin |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20190530 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207762 |
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| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
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| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
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| Strength | 10; 80 |
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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], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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