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  5. NDC Package Code: 11673-426-54 Up And Up Tioconazole 1

NDC Package 11673-426-54 Up And Up Tioconazole 1

Tioconazole Ointment Vaginal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
11673-426-54
Package Description:
1 POUCH in 1 CARTON / 1 APPLICATOR in 1 POUCH / 4.6 g in 1 APPLICATOR
Product Code:
11673-426
Proprietary Name:
Up And Up Tioconazole 1
Non-Proprietary Name:
Tioconazole
Substance Name:
Tioconazole
Usage Information:
•before using this product read the enclosed brochure and instructions on foil packet for complete directions and information•adults and children 12 years and over: •open the foil packet just before use and remove purple cap•insert entire contents of applicator into the vagina at bedtime. Throw applicator away after use.•children under 12 years of age: ask a doctor
11-Digit NDC Billing Format:
11673042654
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Target Corporation
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Vaginal - Administration into the vagina.
Active Ingredient(s):
TIOCONAZOLE 6.5 g/100g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA075915
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-08-2009
Listing Expiration Date:
12-31-2026
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.

Frequently Asked Questions

What is NDC 11673-426-54?

The NDC Packaged Code 11673-426-54 is assigned to a package of 1 pouch in 1 carton / 1 applicator in 1 pouch / 4.6 g in 1 applicator of Up And Up Tioconazole 1, a human over the counter drug labeled by Target Corporation. The product's dosage form is ointment and is administered via vaginal form.

Is NDC 11673-426 included in the NDC Directory?

Yes, Up And Up Tioconazole 1 with product code 11673-426 is active and included in the NDC Directory. The product was first marketed by Target Corporation on July 08, 2009 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11673-426-54?

The 11-digit format is 11673042654. 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
5-3-211673-426-545-4-211673-0426-54