Fenofibrate
- Product NDC
- 50268-310
- 11-digit product format
- 502680310
- Labeler code
- 50268
- Product ID
- 50268-310_9c95f7e9-fc00-ca71-e053-2a95a90a44f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA090856
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 48 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
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 |
|---|
| 50268-310-12 | 50268031012 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-310-12) > 1 TABLET in 1 BLISTER PACK (50268-310-11) | 20 blister pack | 2016-09-19 | 0000-00-00 | No | No | Current |