| NDC Code | 59762-6732-1 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (59762-6732-1) |
|---|
| Product NDC | 59762-6732 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine Besylate And Atorvastatin Calcium |
|---|
| Non-Proprietary Name | Amlodipine Besylate And Atorvastatin Calcium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140404 |
|---|
| End Marketing Date | 20230430 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA021540 |
|---|
| Manufacturer | Greenstone LLC |
|---|
| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
|---|
| Strength | 10; 40 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| 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] |
|---|