FDA.reportPublic FDA data

Allergy Relief

Product NDC
59726-504
11-digit product format
597260504
Labeler code
59726
Product ID
59726-504_40402e5c-c6b4-4b62-8b8e-9f473d1e9311
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine HCl
Dosage form
TABLET
Route
ORAL
Labeler
P & L Development, LLC
Application
ANDA079112
Marketing category
ANDA
Marketing start
2016-03-31
Marketing end
0000-00-00
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
180 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct59726-504DDiscontinued by firm2026-07-31
excluded packagepackage59726-50459726-504-03DDiscontinued by firm2026-07-31
excluded packagepackage59726-50459726-504-12DDiscontinued by firm2026-07-31
excluded packagepackage59726-50459726-504-30DDiscontinued by firm2026-07-31

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

Orange Book products#

Current product rows page 1 of 1 · 6 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A079112-001CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVESFEXOFENADINE HYDROCHLORIDE30MGTABLET / ORAL2012-02-08
A079112-002CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE30MGTABLET / ORAL2012-02-08
A079112-003FEXOFENADINE HYDROCHLORIDE HIVESFEXOFENADINE HYDROCHLORIDE60MGTABLET / ORAL2012-02-08
A079112-004FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE60MGTABLET / ORAL2012-02-08
A079112-005FEXOFENADINE HYDROCHLORIDE HIVESFEXOFENADINE HYDROCHLORIDE180MGTABLET / ORAL2012-02-08
A079112-006FEXOFENADINE HYDROCHLORIDE ALLERGYFEXOFENADINE HYDROCHLORIDE180MGTABLET / ORAL2012-02-08

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 22:54:322026-06A079112-001CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES30MGTABLET / ORAL2012-02-08a50c72e98297…
2026-08-01 22:54:322026-06A079112-002CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY30MGTABLET / ORAL2012-02-08a50c72e98297…
2026-08-01 22:54:322026-06A079112-003FEXOFENADINE HYDROCHLORIDE HIVES60MGTABLET / ORAL2012-02-08a50c72e98297…
2026-08-01 22:54:322026-06A079112-004FEXOFENADINE HYDROCHLORIDE ALLERGY60MGTABLET / ORAL2012-02-08a50c72e98297…
2026-08-01 22:54:322026-06A079112-005FEXOFENADINE HYDROCHLORIDE HIVES180MGTABLET / ORAL2012-02-08a50c72e98297…
2026-08-01 22:54:322026-06A079112-006FEXOFENADINE HYDROCHLORIDE ALLERGY180MGTABLET / ORAL2012-02-08a50c72e98297…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59726-504-032023-06-07C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS
59726-504-122023-06-07C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS
59726-504-302023-06-07C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS
59726-504-032022-01-28C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS
59726-504-122022-01-28C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS
59726-504-302022-01-28C16284748780-1d6a99b39-405b-a426-e053-dadaa90af4c2DRUG FACTS

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59726-504-03597260504033 BLISTER PACK in 1 CARTON (59726-504-03) > 1 TABLET in 1 BLISTER PACK3 blister pack2016-03-310000-00-00NoNoCurrent
59726-504-12597260504121 BOTTLE, PLASTIC in 1 BOX (59726-504-12) > 120 TABLET in 1 BOTTLE, PLASTIC2016-03-310000-00-00NoNoCurrent
59726-504-305972605043030 BLISTER PACK in 1 CARTON (59726-504-30) > 1 TABLET in 1 BLISTER PACK30 blister pack2016-03-310000-00-00NoNoCurrent