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  5. NDC Package Code: 52120-200-10 Ultacan

NDC Package 52120-200-10 Ultacan

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
52120-200-10
Package Description:
100 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)
Product Code:
52120-200
Proprietary Name:
Ultacan
Usage Information:
Ultacan® and Ultacan® forte, an amide local anesthetic containing a vasoconstrictor, are indicated for local, infiltrative, or conductive anesthesia in both simple and complex dental procedures.
11-Digit NDC Billing Format:
52120020010
NDC to RxNorm Crosswalk:
  • RxCUI: 1928853 - articaine hydrochloride 40 MG / EPINEPHrine bitartrate 1:200,000 in 1.7 ML Cartridge
  • RxCUI: 1928853 - 1.7 ML articaine hydrochloride 40 MG/ML / epinephrine bitartrate 0.009 MG/ML Cartridge
  • RxCUI: 1928853 - articaine hydrochloride 40 MG / epinephrine bitartrate 0.009 MG per 1.7 ML Cartridge
  • RxCUI: 1928853 - articaine hydrochloride 40 MG / epinephrine bitartrate 1:200,000 per 1.7 ML Cartridge
  • RxCUI: 1928858 - Ultacan 40 MG / 1:200,000 in 1.7 ML Cartridge
    • Labeler Name:
    Hansamed, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-11-2017
    Listing Expiration Date:
    12-31-2018
    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
    52120-200-0110 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)
    52120-200-0550 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52120-200-10?

    The NDC Packaged Code 52120-200-10 is assigned to a package of 100 cartridge in 1 box / 1.7 ml in 1 cartridge (52120-200-00) of Ultacan, labeled by Hansamed, Inc.. The product's dosage form is and is administered via form.

    Is NDC 52120-200 included in the NDC Directory?

    No, Ultacan with product code 52120-200 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Hansamed, Inc. on July 11, 2017 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52120-200-10?

    The 11-digit format is 52120020010. 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
    5-3-252120-200-105-4-252120-0200-10