| NDC Code | 46708-762-90 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (46708-762-90) |
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| Product NDC | 46708-762 |
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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 | 20250523 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217279 |
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| Manufacturer | Alembic Pharmaceuticals Limited |
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| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
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| Strength | 10; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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