Fenofibrate
- Product NDC
- 0904-6810
- 11-digit product format
- 009046810
- Labeler code
- 0904
- Product ID
- 0904-6810_a53fd075-6f9c-4642-835c-6e3be41b26c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2015-11-23
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0904-6810-04 | 00904681004 | 30 BLISTER PACK in 1 CARTON (0904-6810-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2015-11-23 | 0000-00-00 | No | No | Current |