allergy relief

Product NDC
42507-847
11-digit product format
425070847
Labeler code
42507
Product ID
42507-847_63814542-4e9d-4891-bcfc-e0182eb49651
Type
HUMAN OTC DRUG
Nonproprietary name
fexofenadine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
HyVee Inc
Application
ANDA212971
Marketing category
ANDA
Marketing start
2026-02-25
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
180 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
allergy relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FEXOFENADINE HYDROCHLORIDE180 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2S068B75ZU
Rxcui997420

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b893258d-0942-3d8a-3411-056ea0788ff5Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42507-847-30allergy relief30 in 1 BOTTLETABLET, FILM COATED302
42507-847-39allergy relief1 in 1 CARTONTABLET, FILM COATED12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
997420fexofenadine HCl 180 MG 24 HR Oral TabletPSN54635220-dd44-4baa-b929-9e52deb4c3682
997420fexofenadine hydrochloride 180 MG Oral TabletSCD54635220-dd44-4baa-b929-9e52deb4c3682
997420fexofenadine HCl 180 MG 24 HR Oral TabletSY54635220-dd44-4baa-b929-9e52deb4c3682

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
42507-847-304250708473030 in 1 BOTTLEHistorical
42507-847-39425070847391 BOTTLE in 1 CARTON (42507-847-39) / 30 TABLET, FILM COATED in 1 BOTTLE (42507-847-30) 1 bottle2026-02-25NoNoCurrent