fenofibrate
- Product NDC
- 68071-4320
- 11-digit product format
- 680714320
- Labeler code
- 68071
- Product ID
- 68071-4320_bc974329-510a-24ad-e053-2a95a90ae9ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090715
- Marketing category
- ANDA
- Marketing start
- 2014-09-23
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4320-9 | 68071432009 | 90 TABLET in 1 BOTTLE (68071-4320-9) | 90 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |