Fenofibrate
- Product NDC
- 70518-3370
- 11-digit product format
- 705183370
- Labeler code
- 70518
- Product ID
- 70518-3370_d8c40b7e-baf9-51fb-e053-2995a90a6c2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210670
- Marketing category
- ANDA
- Marketing start
- 2022-02-23
- 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 |
|---|
| 70518-3370-0 | 70518337000 | 30 POUCH in 1 BOX (70518-3370-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-3370-1) | 30 pouch | 2022-02-23 | 0000-00-00 | No | No | Current |