Allergy Relief

Product NDC
85828-192
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Grocery Outlet, Inc.
Application
ANDA211075
Marketing category
ANDA
Substance
FEXOFENADINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
85828-192-033 BLISTER PACK in 1 CARTON (85828-192-03) / 5 TABLET in 1 BLISTER PACK20260218NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
441ce66e-515a-d380-e063-6394a90aec7d1192B-GBR-2026-0218Grocery Outlet, Inc.2026-05-21HUMAN OTC DRUG LABEL3