NDC Package 50580-729-13 Zyrtec

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
50580-729-13
Package Description:
3 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Zyrtec
11-Digit NDC Billing Format:
50580072913
Labeler Name:
Mcneil Consumer Healthcare Div Mcneil-ppc, Inc
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
End Marketing Date:
04-30-2012
Listing Expiration Date:
04-30-2012
Exclude Flag:
D
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
50580-729-011 TABLET, FILM COATED in 1 POUCH
50580-729-021 TABLET, FILM COATED in 1 POUCH
50580-729-0350 POUCH in 1 CARTON / 1 TABLET, FILM COATED in 1 POUCH (50580-729-02)
50580-729-055 BLISTER PACK in 1 PACKAGE / 1 TABLET, FILM COATED in 1 BLISTER PACK
50580-729-141 BOTTLE, PLASTIC in 1 PACKAGE / 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-301 BOTTLE, PLASTIC in 1 PACKAGE / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-451 BOTTLE, PLASTIC in 1 PACKAGE / 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-501 BOTTLE, PLASTIC in 1 PACKAGE / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-512 BOTTLE, PLASTIC in 1 PACKAGE / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-701 BOTTLE, PLASTIC in 1 PACKAGE / 70 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50580-729-7575 TABLET, FILM COATED in 1 PACKAGE, COMBINATION
50580-729-901 BOTTLE, PLASTIC in 1 PACKAGE / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50580-729-13?

The NDC Packaged Code 50580-729-13 is assigned to a package of 3 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack of Zyrtec, labeled by Mcneil Consumer Healthcare Div Mcneil-ppc, Inc. The product's dosage form is and is administered via form.

Is NDC 50580-729 included in the NDC Directory?

No, Zyrtec with product code 50580-729 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Mcneil Consumer Healthcare Div Mcneil-ppc, Inc on January 01, 2008 and its listing in the NDC Directory is set to expire on April 30, 2012 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 50580-729-13?

The 11-digit format is 50580072913. 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
5-3-250580-729-135-4-250580-0729-13