Ultravist
NDC Package 50419-342-41

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Ultravist is ® Injection is an iodinated contrast agent indicated for:. Marketed by Bayer Healthcare Pharmaceuticals Inc., this product is identified by NDC 50419-342 and is authorized under FDA application NDA020220.

Identification & Billing

NDC Package Code
50419-342-41
Package Description
10 VIAL, GLASS in 1 CARTON / 50 mL in 1 VIAL, GLASS
Product Code
11-Digit Billing Format
50419034241

Clinical Specifications

Proprietary Name
Ultravist
Dosage Form
-
Usage Information
ULTRAVIST® Injection is an iodinated contrast agent indicated for:

Regulatory & Marketing

Labeler Name
Bayer Healthcare Pharmaceuticals Inc.
FDA Application #
NDA020220
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-30-2009
End Marketing Date
01-03-2021
Listing Expiration
01-03-2021
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (50419-342). Click a package code to view its specific billing and regulatory data.

10 VIAL, GLASS in 1 CARTON / 50 mL in 1 VIAL, GLASS
10 VIAL, GLASS in 1 CARTON / 100 mL in 1 VIAL, GLASS
10 BOTTLE in 1 PACKAGE / 200 mL in 1 BOTTLE
10 VIAL, GLASS in 1 CARTON / 100 mL in 1 VIAL, GLASS

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 50419-342-41 identifies a specific commercial package of 10 vial, glass in 1 carton / 50 ml in 1 vial, glass of Ultravist, labeled by Bayer Healthcare Pharmaceuticals Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Bayer Healthcare Pharmaceuticals Inc. on December 30, 2009. The current certification is valid through January 03, 2021.

How is this Bayer Healthcare Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50419034241. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
50419-342-41
11-Digit CMS (5-4-2)
50419-0342-41

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.