Home
>
National Drug Code (NDC)
>
Trilipix
Trilipix - 54868-5986-0 - (Fenofibric Acid)
Drug Information of Trilipix
| Product NDC: | 54868-5986 |
| Proprietary Name: | Trilipix |
| Non Proprietary Name: | Fenofibric Acid |
| Active Ingredient(s): | 135 mg/1 & nbsp; Fenofibric Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trilipix
| Product NDC: | 54868-5986 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022224 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090219 |
Package Information of Trilipix
| Package NDC: | 54868-5986-0 |
| Package Description: | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-5986-0) |
NDC Information of Trilipix
| NDC Code | 54868-5986-0 |
| Proprietary Name | Trilipix |
| Package Description | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-5986-0) |
| Product NDC | 54868-5986 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fenofibric Acid |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090219 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FENOFIBRIC ACID |
| Strength Number | 135 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC] |
