Fenofibrate
- Product NDC
- 51407-204
- 11-digit product format
- 514070204
- Labeler code
- 51407
- Product ID
- 51407-204_e808ab5d-61f3-fa10-e053-2995a90a9b11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA200884
- Marketing category
- ANDA
- Marketing start
- 2017-09-07
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 48 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-204 | FENOFIBRATE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 3 | Legacy NDC | 20220908_be2477b3-3e4a-7e85-e053-2995a90a5b63.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-204-90 | 51407020490 | 90 TABLET, FILM COATED in 1 BOTTLE (51407-204-90) | 2021-03-23 | 0000-00-00 | No | No | Current |