FENOFIBRATE
- Product NDC
- 71335-1211
- 11-digit product format
- 713351211
- Labeler code
- 71335
- Product ID
- 71335-1211_fac3a5d2-b7f5-4fd3-a268-c414618cabaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208709
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1211-1 | 71335121101 | 30 TABLET in 1 BOTTLE (71335-1211-1) | 30 tablet | 2019-05-06 | 0000-00-00 | No | No | Current |
| 71335-1211-2 | 71335121102 | 90 TABLET in 1 BOTTLE (71335-1211-2) | 90 tablet | 2019-05-06 | 0000-00-00 | No | No | Current |
| 71335-1211-3 | 71335121103 | 28 TABLET in 1 BOTTLE (71335-1211-3) | 28 tablet | 2019-05-06 | 0000-00-00 | No | No | Current |