Fenofibrate
- Product NDC
- 68071-4289
- 11-digit product format
- 680714289
- Labeler code
- 68071
- Product ID
- 68071-4289_bb78cfa5-577c-8e4e-e053-2a95a90abf83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4289-3 | 68071428903 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4289-3) | 2018-02-15 | 0000-00-00 | No | No | Current |