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  5. NDC Package Code: 50580-726-40 Zyrtec Allergy

NDC Package 50580-726-40 Zyrtec Allergy

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50580-726-40
Package Description:
1 BOTTLE, PLASTIC in 1 PACKAGE / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
50580-726
Proprietary Name:
Zyrtec Allergy
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Adults and children 6 years and overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.adults 65 years and overask a doctorchildren under 6 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor
11-Digit NDC Billing Format:
50580072640
NDC to RxNorm Crosswalk:
  • RxCUI: 1014678 - cetirizine HCl 10 MG Oral Tablet
  • RxCUI: 1014678 - cetirizine hydrochloride 10 MG Oral Tablet
  • RxCUI: 1020026 - ZyrTEC 10 MG Oral Tablet
  • RxCUI: 1020026 - cetirizine hydrochloride 10 MG Oral Tablet [Zyrtec]
  • RxCUI: 1020026 - Zyrtec (cetirizine dihydrochloride 10 MG) Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CETIRIZINE HYDROCHLORIDE 10 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:
    NDA019835
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-01-2008
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50580-726-0350 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
    50580-726-052500 POUCH in 1 CASE / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-2550 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-361 BOTTLE, PLASTIC in 1 PACKAGE / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    50580-726-501 BOTTLE, PLASTIC in 1 PACKAGE / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    50580-726-6675 TABLET, FILM COATED in 1 PACKAGE, COMBINATION
    50580-726-902 BOTTLE, PLASTIC in 1 PACKAGE / 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    50580-726-912500 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-9250 POUCH in 1 TRAY / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-933 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-941 BOTTLE in 1 PACKAGE / 60 TABLET, FILM COATED in 1 BOTTLE
    50580-726-951 BOTTLE in 1 PACKAGE / 90 TABLET, FILM COATED in 1 BOTTLE
    50580-726-965 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH
    50580-726-9714 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50580-726-40?

    The NDC Packaged Code 50580-726-40 is assigned to a package of 1 bottle, plastic in 1 package / 40 tablet, film coated in 1 bottle, plastic of Zyrtec Allergy, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 50580-726 included in the NDC Directory?

    Yes, Zyrtec Allergy with product code 50580-726 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on January 01, 2008 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50580-726-40?

    The 11-digit format is 50580072640. 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
    5-3-250580-726-405-4-250580-0726-40