| NDC Code | 68382-429-77 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68382-429-77) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-429-30) |
|---|
| Product NDC | 68382-429 |
|---|
| 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 | 20190530 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207762 |
|---|
| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
|---|
| Strength | 5; 40 |
|---|
| 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] |
|---|