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Fenofibric Acid
Fenofibric Acid - 53489-677-07 - (Fenofibric Acid)
Drug Information of Fenofibric Acid
| Product NDC: | 53489-677 |
| Proprietary Name: | Fenofibric Acid |
| Non Proprietary Name: | Fenofibric Acid |
| Active Ingredient(s): | 35 mg/1 & nbsp; Fenofibric Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fenofibric Acid
| Product NDC: | 53489-677 |
| Labeler Name: | Mutual Pharmaceutical Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022418 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090831 |
Package Information of Fenofibric Acid
| Package NDC: | 53489-677-07 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (53489-677-07) |
NDC Information of Fenofibric Acid
| NDC Code | 53489-677-07 |
| Proprietary Name | Fenofibric Acid |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (53489-677-07) |
| Product NDC | 53489-677 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fenofibric Acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090831 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Mutual Pharmaceutical Company, Inc. |
| Substance Name | FENOFIBRIC ACID |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC] |
