NDC Code | 68071-3546-9 |
Package Description | 90 TABLET in 1 BOTTLE (68071-3546-9) |
Product NDC | 68071-3546 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Atorvastatin Calcium |
Non-Proprietary Name | Atorvastatin Calcium, Film Coated |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20180618 |
Marketing Category Name | ANDA |
Application Number | ANDA209912 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | ATORVASTATIN CALCIUM TRIHYDRATE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |