Product NDC: | 68180-469 |
Proprietary Name: | Lovastatin |
Non Proprietary Name: | lovastatin |
Active Ingredient(s): | 40 mg/1 & nbsp; lovastatin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68180-469 |
Labeler Name: | Lupin Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078296 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071101 |
Package NDC: | 68180-469-03 |
Package Description: | 1000 TABLET in 1 BOTTLE (68180-469-03) |
NDC Code | 68180-469-03 |
Proprietary Name | Lovastatin |
Package Description | 1000 TABLET in 1 BOTTLE (68180-469-03) |
Product NDC | 68180-469 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lovastatin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20071101 |
Marketing Category Name | ANDA |
Labeler Name | Lupin Pharmaceuticals, Inc. |
Substance Name | LOVASTATIN |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |