Fenofibrate
- Product NDC
- 51407-094
- 11-digit product format
- 514070094
- Labeler code
- 51407
- Product ID
- 51407-094_cb0a5458-4eff-535c-e053-2a95a90a4dc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2005-05-13
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-094-90 | Fenofibrate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-094 | FENOFIBRATE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 8 | Legacy NDC, 1 package rows | 20240907_6dd2e25c-aded-4499-e053-2991aa0a9d60.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-094-90 | 51407009490 | 90 TABLET, FILM COATED in 1 BOTTLE (51407-094-90) | 2018-06-07 | 0000-00-00 | No | No | Current |