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FIBRICOR
FIBRICOR - 13310-101-10 - (Fenofibric Acid)
Drug Information of FIBRICOR
| Product NDC: | 13310-101 |
| Proprietary Name: | FIBRICOR |
| 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 FIBRICOR
| Product NDC: | 13310-101 |
| Labeler Name: | AR Scientific, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022418 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090814 |
Package Information of FIBRICOR
| Package NDC: | 13310-101-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (13310-101-10) |
NDC Information of FIBRICOR
| NDC Code | 13310-101-10 |
| Proprietary Name | FIBRICOR |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (13310-101-10) |
| Product NDC | 13310-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fenofibric Acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090814 |
| Marketing Category Name | NDA |
| Labeler Name | AR Scientific, Inc. |
| Substance Name | FENOFIBRIC ACID |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC] |
