Allergy Relief

Product NDC
11822-9995
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine Hydrochloride 60 mg
Dosage form
TABLET
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA076502
Marketing category
ANDA
Substance
FEXOFENADINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
11822-9995-14 BLISTER PACK in 1 CARTON (11822-9995-1) / 6 TABLET in 1 BLISTER PACK2021-12-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Fexofenadine HCl Tablets USPRite Aid Corporation2025-07-18HUMAN OTC DRUG LABEL6