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Fenofibrate
Fenofibrate - 63304-901-90 - (Fenofibrate)
Drug Information of Fenofibrate
| Product NDC: | 63304-901 |
| Proprietary Name: | Fenofibrate |
| Non Proprietary Name: | Fenofibrate |
| Active Ingredient(s): | 160 mg/1 & nbsp; Fenofibrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fenofibrate
| Product NDC: | 63304-901 |
| Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076635 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060510 |
Package Information of Fenofibrate
| Package NDC: | 63304-901-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (63304-901-90) |
NDC Information of Fenofibrate
| NDC Code | 63304-901-90 |
| Proprietary Name | Fenofibrate |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (63304-901-90) |
| Product NDC | 63304-901 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fenofibrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20060510 |
| Marketing Category Name | ANDA |
| Labeler Name | Ranbaxy Pharmaceuticals Inc. |
| Substance Name | FENOFIBRATE |
| Strength Number | 160 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient] |
