Product NDC: | 0074-6122 |
Proprietary Name: | Tricor |
Non Proprietary Name: | Fenofibrate |
Active Ingredient(s): | 48 mg/1 & nbsp; Fenofibrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0074-6122 |
Labeler Name: | AbbVie Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021656 |
Marketing Category: | NDA |
Start Marketing Date: | 20041105 |
Package NDC: | 0074-6122-90 |
Package Description: | 90 TABLET in 1 BOTTLE (0074-6122-90) |
NDC Code | 0074-6122-90 |
Proprietary Name | Tricor |
Package Description | 90 TABLET in 1 BOTTLE (0074-6122-90) |
Product NDC | 0074-6122 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fenofibrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20041105 |
Marketing Category Name | NDA |
Labeler Name | AbbVie Inc. |
Substance Name | FENOFIBRATE |
Strength Number | 48 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient] |