| NDC Code | 59762-6712-1 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (59762-6712-1) |
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| Product NDC | 59762-6712 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amlodipine Besylate And Atorvastatin Calcium |
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| Non-Proprietary Name | Amlodipine Besylate And Atorvastatin Calcium |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20140404 |
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| End Marketing Date | 20230331 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021540 |
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| Manufacturer | Greenstone LLC |
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| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
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| Strength | 2.5; 40 |
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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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