NDC Code | 0378-4511-93 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4511-93) |
Product NDC | 0378-4511 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amlodipine And Atorvastatin |
Non-Proprietary Name | Amlodipine And Atorvastatin |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20140619 |
Marketing Category Name | ANDA |
Application Number | ANDA200465 |
Manufacturer | Mylan Pharmaceuticals Inc. |
Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
Strength | 2.5; 20 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |