| NDC Code | 16571-139-50 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (16571-139-50) |
|---|
| Product NDC | 16571-139 |
|---|
| 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 | 20231020 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209912 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | ATORVASTATIN CALCIUM TRIHYDRATE |
|---|
| Strength | 80 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
|---|