Fenofibrate
- Product NDC
- 50268-309
- 11-digit product format
- 502680309
- Labeler code
- 50268
- Product ID
- 50268-309_d5cf6c40-2db6-c82a-e053-2a95a90a9aa8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA075868
- Marketing category
- ANDA
- Marketing start
- 2020-11-02
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 134 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50268-309-13 | 50268030913 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-309-13) > 1 CAPSULE in 1 BLISTER PACK (50268-309-11) | 30 blister pack | 2020-11-02 | 0000-00-00 | No | No | Current |