fenofibrate

Product NDC
68071-4182
11-digit product format
680714182
Labeler code
68071
Product ID
68071-4182_bb64320a-6850-396e-e053-2995a90aa8cc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fenofibrate
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA090715
Marketing category
ANDA
Marketing start
2014-09-23
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-4182-26807141820220 TABLET in 1 BOTTLE (68071-4182-2) 20 tablet2017-12-070000-00-00NoNoCurrent
68071-4182-36807141820330 TABLET in 1 BOTTLE (68071-4182-3) 30 tablet2017-12-070000-00-00NoNoCurrent