Fexofenadine Hydrochloride

Product NDC
41250-784
11-digit product format
412500784
Labeler code
41250
Product ID
41250-784_a7506f46-bff9-fa95-be1e-12f70eb31b1a
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Meijer Distribution, Inc
Application
ANDA076502
Marketing category
ANDA
Marketing start
2014-12-29
Marketing end
0000-00-00
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
180 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-784FEXOFENADINE HYDROCHLORIDE TABLET [MEIJER DISTRIBUTION, INC]4Legacy NDC20241101_2fdeb5fb-1e79-5049-d37e-451f7d7db482.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-784-01412500784011 BOTTLE in 1 CARTON (41250-784-01) > 40 TABLET in 1 BOTTLE1 bottle2014-12-290000-00-00NoNoCurrent
41250-784-30412500784301 BOTTLE in 1 CARTON (41250-784-30) > 30 TABLET in 1 BOTTLE1 bottle2014-12-290000-00-00NoNoCurrent
41250-784-90412500784901 BOTTLE in 1 CARTON (41250-784-90) > 90 TABLET in 1 BOTTLE1 bottle2014-12-290000-00-00NoNoCurrent