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  5. NDC Package Code: 82442-300-72 Up And Up Non Drowsy Allergy Relief

NDC Package 82442-300-72 Up And Up Non Drowsy Allergy Relief

Fexofenadine Hydrochloride Tablet, Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
82442-300-72
Package Description:
1 BOTTLE in 1 CARTON / 60 TABLET, COATED in 1 BOTTLE
Product Code:
82442-300
Proprietary Name:
Up And Up Non Drowsy Allergy Relief
Non-Proprietary Name:
Fexofenadine Hydrochloride
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Adults and children 12 years of age and overtake one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hourschildren under 12 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor
11-Digit NDC Billing Format:
82442030072
NDC to RxNorm Crosswalk:
  • RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
  • RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Target Corporation
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • FEXOFENADINE HYDROCHLORIDE 180 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA212971
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-04-2024
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 82442-300-72?

    The NDC Packaged Code 82442-300-72 is assigned to a package of 1 bottle in 1 carton / 60 tablet, coated in 1 bottle of Up And Up Non Drowsy Allergy Relief, a human over the counter drug labeled by Target Corporation. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 82442-300 included in the NDC Directory?

    Yes, Up And Up Non Drowsy Allergy Relief with product code 82442-300 is active and included in the NDC Directory. The product was first marketed by Target Corporation on March 04, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 82442-300-72?

    The 11-digit format is 82442030072. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-282442-300-725-4-282442-0300-72