Home NDC 53187-189 24 Hour Allergy
Product NDC 53187-189
11-digit product format 531870189
Labeler code 53187
Product ID 53187-189_30bdf288-c933-4867-9929-ef702c97ef9d
Type HUMAN OTC DRUG
Nonproprietary name Fexofenadine HCl
Dosage form TABLET
Route ORAL
Labeler LIVE BETTER (The Great Atlantic & Pacific Tea Company)
Application ANDA079112
Marketing category ANDA
Marketing start 2013-03-20
Marketing end 0000-00-00
Substance FEXOFENADINE HYDROCHLORIDE
Active strength 180 mg/1
NDC exclude flag No
Listing certified through 2019-12-31
Current FDA listing Historical FDA.report record 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-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A079112-001 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2012-02-08 A079112-002 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2012-02-08 A079112-003 FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2012-02-08 A079112-004 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2012-02-08 A079112-005 FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2012-02-08 A079112-006 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2012-02-08
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 Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A079112-001 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES 30MG TABLET / ORAL 2012-02-08 a50c72e98297…2026-08-01 22:54:32 2026-06 A079112-002 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2012-02-08 a50c72e98297…2026-08-01 22:54:32 2026-06 A079112-003 FEXOFENADINE HYDROCHLORIDE HIVES 60MG TABLET / ORAL 2012-02-08 a50c72e98297…2026-08-01 22:54:32 2026-06 A079112-004 FEXOFENADINE HYDROCHLORIDE ALLERGY 60MG TABLET / ORAL 2012-02-08 a50c72e98297…2026-08-01 22:54:32 2026-06 A079112-005 FEXOFENADINE HYDROCHLORIDE HIVES 180MG TABLET / ORAL 2012-02-08 a50c72e98297…2026-08-01 22:54:32 2026-06 A079112-006 FEXOFENADINE HYDROCHLORIDE ALLERGY 180MG TABLET / ORAL 2012-02-08 a50c72e98297…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients#