Fenofibrate
- Product NDC
- 0904-7128
- 11-digit product format
- 009047128
- Labeler code
- 0904
- Product ID
- 0904-7128_0a333de0-9c71-41f4-8ae2-e1fcf42253e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7128 | FENOFIBRATE TABLET [MAJOR PHARMACEUTICALS] | 4 | Legacy NDC | 20250316_0a333de0-9c71-41f4-8ae2-e1fcf42253e0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7128-04 | 00904712804 | 30 BLISTER PACK in 1 CARTON (0904-7128-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2020-07-01 | 0000-00-00 | No | No | Current |