Fenoglide
- Product NDC
- 68012-495
- 11-digit product format
- 680120495
- Labeler code
- 68012
- Product ID
- 68012-495_ae9a87e8-23dd-492c-907e-51ea9d58eb97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Santarus, Inc.
- Application
- NDA022118
- Marketing category
- NDA
- Marketing start
- 2010-11-18
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68012-495-07 | 68012049507 | 6 BOTTLE in 1 BOX (68012-495-07) > 7 TABLET in 1 BOTTLE | 6 bottle | 2010-11-18 | 0000-00-00 | No | No | Current |
| 68012-495-90 | 68012049590 | 90 TABLET in 1 BOTTLE (68012-495-90) | 90 tablet | 2010-11-18 | 0000-00-00 | No | No | Current |