FENOFIBRATE
- Product NDC
- 42291-290
- 11-digit product format
- 422910290
- Labeler code
- 42291
- Product ID
- 42291-290_e7b3cc50-62e2-2f0d-e053-2a95a90a76fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA076509
- Marketing category
- ANDA
- Marketing start
- 2015-01-16
- 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
- 2023-12-31
- 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 |
|---|
| 42291-290-30 | 42291029030 | 30 TABLET in 1 BOTTLE (42291-290-30) | 30 tablet | 2015-01-16 | 0000-00-00 | No | No | Current |
| 42291-290-90 | 42291029090 | 90 TABLET in 1 BOTTLE (42291-290-90) | 90 tablet | 2015-01-16 | 0000-00-00 | No | No | Current |