Product NDC: | 45963-633 |
Proprietary Name: | Lovastatin |
Non Proprietary Name: | Lovastatin |
Active Ingredient(s): | 10 mg/1 & nbsp; Lovastatin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45963-633 |
Labeler Name: | Actavis Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075828 |
Marketing Category: | ANDA |
Start Marketing Date: | 20011217 |
Package NDC: | 45963-633-01 |
Package Description: | 60 TABLET in 1 BOTTLE (45963-633-01) |
NDC Code | 45963-633-01 |
Proprietary Name | Lovastatin |
Package Description | 60 TABLET in 1 BOTTLE (45963-633-01) |
Product NDC | 45963-633 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lovastatin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20011217 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Inc. |
Substance Name | LOVASTATIN |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |