Product NDC: | 54868-4601 |
Proprietary Name: | LESCOL XL |
Non Proprietary Name: | fluvastatin sodium |
Active Ingredient(s): | 80 mg/1 & nbsp; fluvastatin sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4601 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021192 |
Marketing Category: | NDA |
Start Marketing Date: | 20020312 |
Package NDC: | 54868-4601-0 |
Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4601-0) |
NDC Code | 54868-4601-0 |
Proprietary Name | LESCOL XL |
Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4601-0) |
Product NDC | 54868-4601 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluvastatin sodium |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20020312 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | FLUVASTATIN SODIUM |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |