Fenoglide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Shore Therapeutics, Inc. The primary component is Fenofibrate.
| Product ID | 52725-490_986c60c0-7d75-11e0-b654-0002a5d5c51b |
| NDC | 52725-490 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Fenoglide |
| Generic Name | Fenofibrate |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-11-18 |
| Marketing Category | NDA / NDA |
| Application Number | NDA022118 |
| Labeler Name | Shore Therapeutics, Inc |
| Substance Name | FENOFIBRATE |
| Active Ingredient Strength | 40 mg/1 |
| Pharm Classes | Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2010-11-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA022118 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-11-18 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| FENOFIBRATE | 40 mg/1 |
| SPL SET ID: | b38489c0-ee7b-11df-b958-0002a5d5c51b |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 68012-490 | Fenoglide | Fenoglide |
| 68012-495 | Fenoglide | Fenoglide |
| 52725-490 | Fenoglide | Fenoglide |
| 52725-495 | Fenoglide | Fenoglide |
| 0093-7755 | Fenofibrate | Fenofibrate |
| 0093-7756 | Fenofibrate | Fenofibrate |
| 0115-0511 | Fenofibrate | FENOFIBRATE |
| 0115-0522 | Fenofibrate | FENOFIBRATE |
| 0115-0533 | Fenofibrate | FENOFIBRATE |
| 0115-1522 | Fenofibrate | Fenofibrate |
| 0115-1523 | Fenofibrate | Fenofibrate |
| 0115-5511 | FENOFIBRATE | FENOFIBRATE |
| 0115-5522 | FENOFIBRATE | FENOFIBRATE |
| 0074-3173 | Tricor | Fenofibrate |
| 0074-3189 | Tricor | Fenofibrate |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FENOGLIDE 77381746 3528941 Live/Registered |
SANTARUS, INC. 2008-01-28 |