Product NDC: | 63629-1464 |
Proprietary Name: | Lovastatin |
Non Proprietary Name: | Lovastatin |
Active Ingredient(s): | 20 mg/1 & nbsp; Lovastatin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-1464 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075551 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090615 |
Package NDC: | 63629-1464-2 |
Package Description: | 100 TABLET in 1 BOTTLE (63629-1464-2) |
NDC Code | 63629-1464-2 |
Proprietary Name | Lovastatin |
Package Description | 100 TABLET in 1 BOTTLE (63629-1464-2) |
Product NDC | 63629-1464 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lovastatin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090615 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | LOVASTATIN |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |