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  5. NDC Package Code: 50580-779-12 Zyrtec

NDC Package 50580-779-12 Zyrtec

Cetirizine Hydrochloride Capsule, Liquid Filled 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:
50580-779-12
Package Description:
1 BOTTLE in 1 PACKAGE / 12 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
50580-779
Proprietary Name:
Zyrtec
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Adults and children 6 years and overone 10 mg capsule once daily; do not take more than one 10 mg capsule 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:
50580077912
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1014675 - cetirizine HCl 10 MG 24HR Oral Capsule
  • RxCUI: 1014675 - cetirizine hydrochloride 10 MG Oral Capsule
  • RxCUI: 1014675 - cetirizine HCl 10 MG 24 HR Oral Capsule
  • RxCUI: 1020023 - ZyrTEC 10 MG Oral Capsule
  • RxCUI: 1020023 - cetirizine hydrochloride 10 MG Oral Capsule [Zyrtec]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
    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:
    NDA022429
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-08-2010
    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
    50580-779-251 BOTTLE in 1 PACKAGE / 25 CAPSULE, LIQUID FILLED in 1 BOTTLE
    50580-779-401 BOTTLE in 1 PACKAGE / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
    50580-779-6565 CAPSULE, LIQUID FILLED in 1 PACKAGE, COMBINATION

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50580-779-12?

    The NDC Packaged Code 50580-779-12 is assigned to a package of 1 bottle in 1 package / 12 capsule, liquid filled in 1 bottle of Zyrtec, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is capsule, liquid filled and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 50580-779 included in the NDC Directory?

    Yes, Zyrtec with product code 50580-779 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on February 08, 2010 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 NDC billing unit for package 50580-779-12?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 50580-779-12?

    The 11-digit format is 50580077912. 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
    5-3-250580-779-125-4-250580-0779-12