E-Z-HD

This brand name is authorized in United States. It is also authorized in Estonia, Israel, South Africa, UK.

Active ingredients

The drug E-Z-HD contains one active pharmaceutical ingredient (API):

1	Barium sulfate UNII 25BB7EKE2E - BARIUM SULFATE
	Barium sulfate is inert and has no pharmacological action. It serves only as a radiopaque substance to opacify the gastro-intestinal tract during X-ray examinations.
	Read more about Barium sulfate

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
E-Z-HD Powder for oral suspension	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
V08BA01	Barium sulfate with suspending agents	V Various → V08 Contrast media → V08B X-ray contrast media, non-iodinated → V08BA Barium sulfate containing X-ray contrast media
Discover more medicines within V08BA01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1298640, 1346037, 1764828
GB	Medicines & Healthcare Products Regulatory Agency	309259, 88038
IL	מִשְׂרַד הַבְּרִיאוּת	6973
US	FDA, National Drug Code	32909-764
ZA	Health Products Regulatory Authority	P/28/277