| NDC Code | 46708-760-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (46708-760-30) |
|---|
| Product NDC | 46708-760 |
|---|
| 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 | 20250523 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA217279 |
|---|
| Manufacturer | Alembic Pharmaceuticals Limited |
|---|
| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE |
|---|
| Strength | 5; 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] |
|---|