DIABACT UBT

This brand name is authorized in Austria, Finland, Hong Kong, Ireland, United Kingdom

Active ingredients

The drug DIABACT UBT contains one active pharmaceutical ingredient (API):

1 Urea ¹³C
UNII W6KX9E6D8X - UREA C-13

13C-urea is administered in the course of the breath test. After oral ingestion the labelled urea reaches the gastric mucosa. In the presence of Helicobacter pylori the 13C-urea is metabolised by the enzyme urease of Helicobacter pylori.

Read about Urea ¹³C

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
DIABACT UBT Tablet Health Products Regulatory Authority (IE) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
V04CX05 V Various → V04 Diagnostic agents → V04C Other diagnostic agents → V04CX Other diagnostic agents
Discover more medicines within V04CX05

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 016874, 016937
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 93843, 93844
Country: HK Department of Health Drug Office Identifier(s): 49351

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