Fenofibrate
- Product NDC
- 60760-660
- 11-digit product format
- 607600660
- Labeler code
- 60760
- Product ID
- 60760-660_b7893c4e-2d19-33e5-e053-2995a90a4d71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St Mary's Medical Park Pharmacy
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- 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
- 2021-12-31
- 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 |
|---|
| 60760-660-30 | 60760066030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-660-30) | 2019-06-05 | 0000-00-00 | No | No | Current |