FDA.reportPublic FDA data

Fexofenadine hydrochloride

Product NDC
0363-0097
Requested package NDC
0363-0097-55
11-digit product format
003630097
Labeler code
0363
Product ID
0363-0097_45b3aac8-2ad2-4cfa-858e-9cb8528292e6
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Walgreen CO
Application
ANDA202039
Marketing category
ANDA
Marketing start
2015-01-15
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

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0363-00970363-0097-55IInactivated by FDA2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 3 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A202039-001CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE30MGTABLET / ORAL2014-11-19
A202039-002FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE60MGTABLET / ORAL2014-11-19
A202039-003FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE180MGTABLET / ORAL2014-11-19

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A202039-001CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY30MGTABLET / ORAL2014-11-19a50c72e98297…
2026-08-01 22:54:322026-06A202039-002FEXOFENADINE HYDROCHLORIDE ALLERGY60MGTABLET / ORAL2014-11-19a50c72e98297…
2026-08-01 22:54:322026-06A202039-003FEXOFENADINE HYDROCHLORIDE ALLERGY180MGTABLET / ORAL2014-11-19a50c72e98297…

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Fexofenadine hydrochlorideFEXOFENADINE HYDROCHLORIDE7-elevend5914c05-e8db-4c79-82d0-a279d13041182019-06-20WarningsExact identifier
application applno (ANDA): 202039
application number: ANDA202039

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-0097-532023-01-30C16284748780-1f386c649-cce1-0266-e053-dadaa90a7c1add7a5c55-f834-4aa2-8cdf-a62154ce7dde
0363-0097-552023-01-30C16284748780-1f386c649-cce1-0266-e053-dadaa90a7c1add7a5c55-f834-4aa2-8cdf-a62154ce7dde

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0097-53Fexofenadine hydrochloride15 in 1 BLISTER PACKTABLET, FILM COATED153
0363-0097-53Fexofenadine hydrochloride1 in 1 CARTONTABLET, FILM COATED13
0363-0097-55Fexofenadine hydrochloride1 in 1 CARTONTABLET, FILM COATED13
0363-0097-55Fexofenadine hydrochloride5 in 1 BLISTER PACKTABLET, FILM COATED53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0097FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [WALGREEN CO]3Legacy NDC, 4 package rows20190911_dd7a5c55-f834-4aa2-8cdf-a62154ce7dde.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
997420fexofenadine HCl 180 MG 24 HR Oral TabletPSNdd7a5c55-f834-4aa2-8cdf-a62154ce7dde3
997501fexofenadine HCl 60 MG Oral TabletPSNdd7a5c55-f834-4aa2-8cdf-a62154ce7dde3
997420fexofenadine hydrochloride 180 MG Oral TabletSCDdd7a5c55-f834-4aa2-8cdf-a62154ce7dde3
997501fexofenadine hydrochloride 60 MG Oral TabletSCDdd7a5c55-f834-4aa2-8cdf-a62154ce7dde3
997420fexofenadine HCl 180 MG 24 HR Oral TabletSYdd7a5c55-f834-4aa2-8cdf-a62154ce7dde3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-0097-55003630097551 BLISTER PACK in 1 CARTON (0363-0097-55) > 5 TABLET, FILM COATED in 1 BLISTER PACK1 blister pack2015-01-150000-00-00NoNoCurrent