Easy-ceft
NDC Package 79144-101-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Easy-ceft is iNDICATIONS AND USAGEBefore instituting treatment with Ceftriaxone for Injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Marketed by American Health Rx, Llc, this product is identified by NDC 79144-101.

Identification & Billing

NDC Package Code
79144-101-01
Package Description
1 KIT in 1 BOX * 25 VIAL in 1 CARTON (44567-701-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product Code
79144-101
11-Digit Billing Format
79144010101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Easy-ceft 1g
Dosage Form
-
Usage Information
INDICATIONS AND USAGEBefore instituting treatment with Ceftriaxone for Injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Therapy may be instituted prior to obtaining results of susceptibility testing. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Ceftriaxone for Injection, USP is indicated for the treatment of the following infections when caused by susceptible organisms:

Regulatory & Marketing

Labeler Name
American Health Rx, Llc
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
06-15-2021
Listing Expiration
12-31-2022
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 79144-101-01 identifies a specific commercial package of 1 kit in 1 box * 25 vial in 1 carton (44567-701-25) / 1 injection, powder, for solution in 1 vial of Easy-ceft 1g, labeled by American Health Rx, Llc. 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 American Health Rx, Llc on June 15, 2021. The current certification is valid through December 31, 2022.

How is this American Health Rx, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79144010101. 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)
79144-101-01
11-Digit CMS (5-4-2)
79144-0101-01

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