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  5. NDC Package Code: 32909-750-03 E-z-paque

NDC Package 32909-750-03 E-z-paque

Barium Sulfate Powder, For Suspension Oral - 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:
32909-750-03
Package Description:
24 BOTTLE, PLASTIC in 1 CARTON / 176 g in 1 BOTTLE, PLASTIC
Product Code:
32909-750
Proprietary Name:
E-z-paque
Non-Proprietary Name:
Barium Sulfate
Substance Name:
Barium Sulfate
Usage Information:
E-Z-PAQUE is indicated for use in single contrast radiographic examinations of the esophagus, stomach, duodenum and small bowel to visualize the gastrointestinal tract (GI) in adult and pediatric patients.
11-Digit NDC Billing Format:
32909075003
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
176 GM
Product Type:
Human Prescription Drug
Labeler Name:
E-z-em Canada Inc
Dosage Form:
Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
BARIUM SULFATE 960 mg/g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA208036
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
06-01-2017
Listing Expiration Date:
12-31-2025
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 32909-750-03?

The NDC Packaged Code 32909-750-03 is assigned to a package of 24 bottle, plastic in 1 carton / 176 g in 1 bottle, plastic of E-z-paque, a human prescription drug labeled by E-z-em Canada Inc. The product's dosage form is powder, for suspension and is administered via oral form.This product is billed per "GM" gram and contains an estimated amount of 176 billable units per package.

Is NDC 32909-750 included in the NDC Directory?

Yes, E-z-paque with product code 32909-750 is active and included in the NDC Directory. The product was first marketed by E-z-em Canada Inc on June 01, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 32909-750-03?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 176.

What is the 11-digit format for NDC 32909-750-03?

The 11-digit format is 32909075003. 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
5-3-232909-750-035-4-232909-0750-03