Fenofibrate
- Product NDC
- 70518-1988
- 11-digit product format
- 705181988
- Labeler code
- 70518
- Product ID
- 70518-1988_c572ecfd-1d96-2bc0-e053-2995a90ae3cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2019-03-27
- 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
- 2022-12-31
- 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 |
|---|
| 70518-1988-0 | 70518198800 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1988-0) | 90 tablet | 2019-03-27 | 0000-00-00 | No | No | Current |