Product NDC: | 55111-123 |
Proprietary Name: | Atorvastatin Calcium |
Non Proprietary Name: | Atorvastatin Calcium |
Active Ingredient(s): | 40 mg/1 & nbsp; Atorvastatin Calcium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55111-123 |
Labeler Name: | Dr. Reddy's Laboratories Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091650 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120717 |
Package NDC: | 55111-123-60 |
Package Description: | 60 TABLET in 1 BOTTLE (55111-123-60) |
NDC Code | 55111-123-60 |
Proprietary Name | Atorvastatin Calcium |
Package Description | 60 TABLET in 1 BOTTLE (55111-123-60) |
Product NDC | 55111-123 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Atorvastatin Calcium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120717 |
Marketing Category Name | ANDA |
Labeler Name | Dr. Reddy's Laboratories Limited |
Substance Name | ATORVASTATIN CALCIUM |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |