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Fenofibrate
Fenofibrate - 68084-635-21 - (Fenofibrate)
Drug Information of Fenofibrate
| Product NDC: | 68084-635 |
| Proprietary Name: | Fenofibrate |
| 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) |
Labeler Information of Fenofibrate
| Product NDC: | 68084-635 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090856 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130206 |
Package Information of Fenofibrate
| Package NDC: | 68084-635-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-635-21) > 10 TABLET in 1 BLISTER PACK (68084-635-11) |
NDC Information of Fenofibrate
| NDC Code | 68084-635-21 |
| Proprietary Name | Fenofibrate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-635-21) > 10 TABLET in 1 BLISTER PACK (68084-635-11) |
| Product NDC | 68084-635 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fenofibrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130206 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| 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] |
