NDC Package 11673-571-87 Up And Up Allergy Relief

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
11673-571-87
Package Description:
1 BOTTLE in 1 CARTON / 300 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Up And Up Allergy Relief
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:
11673057187
NDC to RxNorm Crosswalk:
Labeler Name:
Target Corporation
Sample Package:
No
FDA Application Number:
ANDA076447
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-13-2011
Listing Expiration Date:
12-31-2023
Exclude Flag:
I
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
11673-571-011 BOTTLE in 1 CARTON / 70 TABLET, FILM COATED in 1 BOTTLE
11673-571-2215 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
11673-571-3360 TABLET, FILM COATED in 1 BOTTLE
11673-571-391 BOTTLE in 1 CARTON / 30 TABLET, FILM COATED in 1 BOTTLE
11673-571-471 BOTTLE in 1 CARTON / 150 TABLET, FILM COATED in 1 BOTTLE
11673-571-491 BOTTLE in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE
11673-571-751 BOTTLE in 1 CARTON / 90 TABLET, FILM COATED in 1 BOTTLE
11673-571-762 BOTTLE in 1 CARTON / 60 TABLET, FILM COATED in 1 BOTTLE
11673-571-951 BOTTLE in 1 CARTON / 45 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 11673-571-87?

The NDC Packaged Code 11673-571-87 is assigned to a package of 1 bottle in 1 carton / 300 tablet, film coated in 1 bottle of Up And Up Allergy Relief, labeled by Target Corporation. The product's dosage form is and is administered via form.

Is NDC 11673-571 included in the NDC Directory?

No, Up And Up Allergy Relief with product code 11673-571 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Target Corporation on April 13, 2011 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11673-571-87?

The 11-digit format is 11673057187. 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
5-3-211673-571-875-4-211673-0571-87