Fenofibrate
- Product NDC
- 70934-591
- 11-digit product format
- 709340591
- Labeler code
- 70934
- Product ID
- 70934-591_ab986cb7-32fb-992b-e053-2a95a90a0b60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2020-03-02
- Marketing end
- 2022-05-31
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 70934-591-30 | 70934059130 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-591-30) | 30 tablet | 2020-03-02 | 2022-05-31 | No | No | Current |