Fenofibrate
- Product NDC
- 70518-0700
- 11-digit product format
- 705180700
- Labeler code
- 70518
- Product ID
- 70518-0700_bf8badb2-af48-97d1-e053-2995a90ae8eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2017-08-18
- 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
- 2022-12-31
- 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 |
|---|
| 70518-0700-0 | 70518070000 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0700-0) | 90 tablet | 2017-08-18 | 0000-00-00 | No | No | Current |