Fenofibrate
- Product NDC
- 50090-4121
- 11-digit product format
- 500904121
- Labeler code
- 50090
- Product ID
- 50090-4121_fb34006b-63eb-4946-834c-032bb338bc3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075753
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- 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
- 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 |
|---|
| 50090-4121-0 | 50090412100 | 90 CAPSULE in 1 BOTTLE (50090-4121-0) | 90 capsule | 2019-02-02 | 0000-00-00 | No | No | Current |