NDC Package 11673-900-34 Up And Up Anti Diarrheal

Loperamide Hcl Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

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:
11673-900-34
Package Description:
240 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Up And Up Anti Diarrheal
Non-Proprietary Name:
Loperamide Hcl
Substance Name:
Loperamide Hydrochloride
Usage Information:
See also Warning section. This medication is used to treat sudden diarrhea (including traveler's diarrhea). It works by slowing down the movement of the gut. This decreases the number of bowel movements and makes the stool less watery. Loperamide is also used to reduce the amount of discharge in patients who have had an ileostomy. It is also used to treat ongoing diarrhea in people with inflammatory bowel disease. Loperamide treats only the symptoms, not the cause of the diarrhea (e.g., infection). Treatment of other symptoms and the cause of the diarrhea should be determined by your doctor.
11-Digit NDC Billing Format:
11673090034
NDC to RxNorm Crosswalk:
  • RxCUI: 1250685 - loperamide HCl 1 MG in 7.5 mL Oral Suspension
  • RxCUI: 1250685 - loperamide hydrochloride 0.133 MG/ML Oral Suspension
  • RxCUI: 1250685 - loperamide HCl 1 MG per 7.5 ML Oral Solution
  • RxCUI: 1250685 - loperamide hydrochloride 1 MG per 7.5 ML Oral Suspension
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Target Corporation
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA091292
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-26-2016
    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.

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    Frequently Asked Questions

    What is NDC 11673-900-34?

    The NDC Packaged Code 11673-900-34 is assigned to a package of 240 ml in 1 bottle of Up And Up Anti Diarrheal, a human over the counter drug labeled by Target Corporation. The product's dosage form is suspension and is administered via oral form.

    Is NDC 11673-900 included in the NDC Directory?

    Yes, Up And Up Anti Diarrheal with product code 11673-900 is active and included in the NDC Directory. The product was first marketed by Target Corporation on February 26, 2016 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 11673-900-34?

    The 11-digit format is 11673090034. 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
    5-3-211673-900-345-4-211673-0900-34