Tricor
- Product NDC
- 0074-3173
- 11-digit product format
- 000743173
- Labeler code
- 0074
- Product ID
- 0074-3173_7d6fd4ec-c931-458a-8687-fd3a96dfda2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA021656
- Marketing category
- NDA
- Marketing start
- 2016-02-05
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 48 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
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0074-3173 | TRICOR (FENOFIBRATE) TABLET [ABBVIE INC.] | 1516 | Legacy NDC | 20241122_b693e68d-f812-4993-54b6-852e3517c344.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0074-3173-90 | 00074317390 | 90 TABLET in 1 BOTTLE (0074-3173-90) | 90 tablet | 2016-02-05 | 0000-00-00 | No | No | Current |