Allergy Relief

Product NDC
53943-392
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
DISCOUNT DRUG MART
Application
ANDA211075
Marketing category
ANDA
Substance
FEXOFENADINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
53943-392-041 BOTTLE, PLASTIC in 1 CARTON (53943-392-04) / 30 TABLET in 1 BOTTLE, PLASTIC2021-09-01NoHistorical
53943-392-061 BOTTLE, PLASTIC in 1 CARTON (53943-392-06) / 45 TABLET in 1 BOTTLE, PLASTIC2021-09-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1192B-DDM-2021-1127DISCOUNT DRUG MART2021-11-30HUMAN OTC DRUG LABEL2