Drug Information

Product NDC: 10361-778

Proprietary Name: E-Z-Disk

Non Proprietary Name: barium sulfate

Active Ingredient(s):
  • 700 mg/1 BARIUM SULFATE

Administration Route(s): ORAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Radiographic Contrast Agent [EPC];
  • X-Ray Contrast Activity [MoA]

Labeler Information

Labeler Name: E-Z-EM, INC.
FDA Application Number:
Start Marketing Date:2/1/2009

Package Information

No. Package Code Package Description Billing Unit
110361-778-31100 TABLET in 1 BOTTLE, GLASS (10361-778-31)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC10361-778The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEE-Z-DiskThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEbarium sulfateThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEE-Z-EM, INC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBARIUM SULFATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PHARM CLASSESRadiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA] 

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This page was last updated on: 4/12/2024