Fenofibrate
- Product NDC
- 51407-090
- 11-digit product format
- 514070090
- Labeler code
- 51407
- Product ID
- 51407-090_c55e9d1d-d4fa-8d21-e053-2a95a90a0226
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075753
- Marketing category
- ANDA
- Marketing start
- 2002-09-03
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 67 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 |
|---|
| 51407-090 | FENOFIBRATE CAPSULE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 8 | Legacy NDC | 20230420_6e79dd5a-7f8e-53a9-e053-2991aa0a1ecd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-090-90 | 51407009090 | 90 CAPSULE in 1 BOTTLE (51407-090-90) | 90 capsule | 2018-06-07 | 0000-00-00 | No | No | Current |