Fenofibrate
- Product NDC
- 71205-366
- 11-digit product format
- 712050366
- Labeler code
- 71205
- Product ID
- 71205-366_35b7e5e3-2c66-4441-9cda-9370264d3d3b
- 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
- 54 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 |
|---|
| 71205-366 | FENOFIBRATE TABLET [PROFICIENT RX LP] | 1 | Legacy NDC | 20191128_35b7e5e3-2c66-4441-9cda-9370264d3d3b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-366-30 | 71205036630 | 30 TABLET in 1 BOTTLE (71205-366-30) | 30 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |
| 71205-366-60 | 71205036660 | 60 TABLET in 1 BOTTLE (71205-366-60) | 60 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |
| 71205-366-90 | 71205036690 | 90 TABLET in 1 BOTTLE (71205-366-90) | 90 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |