Home NDC 72036-292 Allergy Relief
Product NDC 72036-292
11-digit product format 720360292
Labeler code 72036
Product ID 72036-292_2433748b-8030-b5d9-e063-6394a90a2e28
Type HUMAN OTC DRUG
Nonproprietary name Fexofenadine Hydrochloride
Dosage form TABLET
Route ORAL
Labeler HARRIS TEETER
Application ANDA211075
Marketing category ANDA
Marketing start 2021-09-06
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 2026-12-31
Current FDA listing Yes NDC auxiliary status# Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table Dataset Scope Product NDC Package NDC Code Status Reporting period Source date excluded package package 72036-292 72036-292-06 D Discontinued by firm 2026-07-31
Orange Book products# Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A211075-001 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2019-10-18 A211075-002 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2019-10-18
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.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed do not take at the same time as aluminum or magnesium antacids do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Additional Listing Data#
Finished product Yes
Brand name base Allergy Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FEXOFENADINE HYDROCHLORIDE 180 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii 2S068B75ZU Rxcui 997420
DailyMed Product Concepts# DailyMed Package Descriptions# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72036-292 ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET [HARRIS TEETER] 4 Current NDC, Legacy NDC, 8 package rows 20241013_c4f9e849-f286-4167-e053-2a95a90a38f9.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72036-292-03 72036029203 3 BLISTER PACK in 1 CARTON (72036-292-03) / 5 TABLET in 1 BLISTER PACK 3 blister pack 2021-09-06 0000-00-00 No No Current 72036-292-04 72036029204 1 BOTTLE, PLASTIC in 1 CARTON (72036-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC 2021-09-06 0000-00-00 No No Current 72036-292-06 72036029206 1 BOTTLE, PLASTIC in 1 CARTON (72036-292-06) > 45 TABLET in 1 BOTTLE, PLASTIC 2021-09-06 0000-00-00 No No Current 72036-292-09 72036029209 1 BOTTLE, PLASTIC in 1 CARTON (72036-292-09) / 90 TABLET in 1 BOTTLE, PLASTIC 2021-09-06 0000-00-00 No No Current