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  4. NDC Product Code: 52120-200 Ultacan

NDC 52120-200 Ultacan

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52120-200?
  4. Ultacan Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52120-200
Proprietary Name:
Ultacan
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hansamed, Inc.
Labeler Code:
52120
Product Label ID:
e005e3da-142d-4eba-a0c0-35e05b234130
Start Marketing Date: [9]
07-11-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52120-200-01

Package Description: 10 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)

NDC Code 52120-200-05

Package Description: 50 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)

NDC Code 52120-200-10

Package Description: 100 CARTRIDGE in 1 BOX / 1.7 mL in 1 CARTRIDGE (52120-200-00)

Product Details

What is NDC 52120-200?

The NDC code 52120-200 is assigned by the FDA to the product Ultacan which is product labeled by Hansamed, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 52120-200-01 10 cartridge in 1 box / 1.7 ml in 1 cartridge (52120-200-00), 52120-200-05 50 cartridge in 1 box / 1.7 ml in 1 cartridge (52120-200-00), 52120-200-10 100 cartridge in 1 box / 1.7 ml in 1 cartridge (52120-200-00). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Ultacan?

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.

Which are Ultacan UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Ultacan Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Ultacan?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".