Trilipix
- Product NDC
- 0074-9642
- 11-digit product format
- 000749642
- Labeler code
- 0074
- Product ID
- 0074-9642_5ba21517-084d-2b89-eaa9-d53a00f9c95f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibric Acid
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA022224
- Marketing category
- NDA
- Marketing start
- 2008-12-15
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRIC ACID
- Active strength
- 45 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 |
|---|
| 0074-9642-90 | 00074964290 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-9642-90) | 2008-12-15 | 0000-00-00 | No | No | Current |