Fenofibrate
- Product NDC
- 16714-738
- 11-digit product format
- 167140738
- Labeler code
- 16714
- Product ID
- 16714-738_fb55b9da-1b95-403f-a2ea-85bd92186baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA205118
- Marketing category
- ANDA
- Marketing start
- 2017-07-15
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-738-01 | 16714073801 | 90 TABLET, COATED in 1 BOTTLE (16714-738-01) | 2017-07-15 | 0000-00-00 | No | No | Current |