FENOFIBRATE
- Product NDC
- 63629-7151
- 11-digit product format
- 636297151
- Labeler code
- 63629
- Product ID
- 63629-7151_7a15b967-b7ec-418e-8e4f-16dfc9fc2e17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076509
- Marketing category
- ANDA
- Marketing start
- 2010-02-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7151-1 | 63629715101 | 30 TABLET in 1 BOTTLE (63629-7151-1) | 30 tablet | 2016-12-08 | 0000-00-00 | No | No | Current |