Fenofibric Acid
- Product NDC
- 60429-432
- 11-digit product format
- 604290432
- Labeler code
- 60429
- Product ID
- 60429-432_a01ed6e6-24ba-9593-e053-2995a90a9837
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibric Acid
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA201573
- Marketing category
- ANDA
- Marketing start
- 2013-07-18
- Marketing end
- 0000-00-00
- Substance
- CHOLINE FENOFIBRATE
- Active strength
- 135 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-432-90 | 60429043290 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60429-432-90) | 2016-01-12 | 0000-00-00 | No | No | Current |