DASSELTA

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, Germany, Hong Kong SAR China, Ireland, Italy, Lithuania, Poland, Romania, Spain.

Active ingredients

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

1	Desloratadine UNII FVF865388R - DESLORATADINE
	Desloratadine is a non-sedating, long-acting histamine antagonist with selective peripheral H1-receptor antagonist activity. After oral administration, desloratadine selectively blocks peripheral histamine Η1-receptors because the substance is excluded from entry to the central nervous system.
	Read more about Desloratadine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DASSELTA Film-coated tablet	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

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

ATC Group		Classification
R06AX27	Desloratadine	R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AX Other antihistamines for systemic use
Discover more medicines within R06AX27

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	09435165, 09435171, 09435188, 09691997, 09692005, 09884532, 09884549, 09884555, 10061793, 10061818, 10543753, 10543782, 17881855
EE	Ravimiamet	1550764, 1550775, 1550786, 1550797, 1550809, 1550810, 1550821, 1550832
ES	Centro de información online de medicamentos de la AEMPS	111739003
FI	Lääkealan turvallisuus- ja kehittämiskeskus	188829, 422099, 571063
HK	Department of Health Drug Office	64326
IE	Health Products Regulatory Authority	35810
IT	Agenzia del Farmaco	041725033
LT	Valstybinė vaistų kontrolės tarnyba	1064185, 1064186, 1064187, 1064188, 1064189, 1064190, 1064191, 1064192
PL	Rejestru Produktów Leczniczych	100087446
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W58162001, W58162002, W58162003, W58162004, W58162005, W58162006, W58162007, W58162008