Trilipix
- Product NDC
- 0074-3161
- 11-digit product format
- 000743161
- Labeler code
- 0074
- Product ID
- 0074-3161_45d3b5e3-12f2-486c-87b6-d2e529e5017c
- 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
- 2016-09-12
- 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
- 2023-12-31
- 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 |
|---|
| 0074-3161-90 | 00074316190 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-3161-90) | 2016-09-12 | 0000-00-00 | No | No | Current |