Fenofibrate
- Product NDC
- 63187-681
- 11-digit product format
- 631870681
- Labeler code
- 63187
- Product ID
- 63187-681_cee81634-9e3d-46e7-a42b-a17562bafa59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2015-11-23
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-681 | FENOFIBRATE TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191121_1d167b24-eb16-48ea-8a97-048cfad6ba62.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-681-30 | 63187068130 | 30 TABLET in 1 BOTTLE (63187-681-30) | 30 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |
| 63187-681-60 | 63187068160 | 60 TABLET in 1 BOTTLE (63187-681-60) | 60 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |
| 63187-681-90 | 63187068190 | 90 TABLET in 1 BOTTLE (63187-681-90) | 90 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |