TUBERSOL

This brand name is authorized in Canada, Israel, New Zealand, United States

Active ingredients

The drug TUBERSOL contains one active pharmaceutical ingredient (API):

1 Tuberculin UNII I7L8FKN87J - TUBERCULIN PURIFIED PROTEIN DERIVATIVE

Tuberculin PPD is indicated for the detection of a delayed hypersensitivity reaction to tuberculin as an aid in the detection of infection with Mycobacterium tuberculosis. Read about Tuberculin

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
TUBERSOL Solution for injection	FDA, National Drug Code (US)	MPI, US: SPL/Old

Medicine classification

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

ATC code	Group title	Classification
V04CF01	Tuberculin	V Various → V04 Diagnostic agents → V04C Other diagnostic agents → V04CF Tuberculosis diagnostics
Discover more medicines within V04CF01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: CA	Health Products and Food Branch	Identifier(s): 00317268
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 6970
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 2238
Country: US	FDA, National Drug Code	Identifier(s): 49281-752, 50090-0261