fenofibrate
- Product NDC
- 71610-027
- 11-digit product format
- 716100027
- Labeler code
- 71610
- Product ID
- 71610-027_84b62471-43ba-4761-92cf-17865209c8e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA090715
- Marketing category
- ANDA
- Marketing start
- 2014-08-13
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71610-027 | FENOFIBRATE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 2 | Legacy NDC | 20180127_75714311-1423-4ba0-a89b-5a06742836c7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-027-83 | 71610002783 | 3600 TABLET in 1 BOTTLE (71610-027-83) | 3600 tablet | 2016-11-07 | 0000-00-00 | No | No | Current |