Fenofibrate
- Product NDC
- 70934-298
- 11-digit product format
- 709340298
- Labeler code
- 70934
- Product ID
- 70934-298_b7b407d0-c110-6d67-e053-2a95a90ac38f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2019-03-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-298-60 | 70934029860 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-298-60) | 2019-03-01 | 0000-00-00 | No | No | Current |