| Product NDC: | 55154-6966 |
| 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: | 55154-6966 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021656 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041105 |
| Package NDC: | 55154-6966-4 |
| Package Description: | 90 POUCH in 1 CARTON (55154-6966-4) > 1 TABLET in 1 POUCH (55154-6966-6) |
| NDC Code | 55154-6966-4 |
| Proprietary Name | TRICOR |
| Package Description | 90 POUCH in 1 CARTON (55154-6966-4) > 1 TABLET in 1 POUCH (55154-6966-6) |
| Product NDC | 55154-6966 |
| 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 | Cardinal Health |
| 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] |