RUPAFIN

This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Estonia, Germany, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, Poland, Singapore, Spain, Turkey.

Active ingredients

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

1	Rupatadine UNII XJ6OT32M93 - RUPATADINE FUMARATE
	Rupatadine is a second-generation antihistamine, long-acting histamine antagonist, with selective peripheral H1-receptor antagonist activity. Some of the metabolites (desloratadine and its hydroxylated metabolites) retain an antihistaminic activity and may partially contribute to the overall efficacy of the drug.
	Read more about Rupatadine

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

ATC Group		Classification
R06AX28	Rupatadine	R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AX Other antihistamines for systemic use
Discover more medicines within R06AX28

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
BR	Câmara de Regulação do Mercado de Medicamentos	552919110082817, 552919110082917
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00114666, 02833951, 05454705, 08922472, 08922584, 08922590, 09534660, 09534677, 09534683, 12448898, 12600917, 12600923, 12600952, 12653351, 12653368, 12653374
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	4330-MEE-0818, 4423-MEE-1018
EE	Ravimiamet	1269952, 1269963, 1269974, 1269985, 1269996, 1270000, 1270011, 1270022, 1505629
ES	Centro de información online de medicamentos de la AEMPS	64053, 75666, BE272045
IL	מִשְׂרַד הַבְּרִיאוּת	8535, 9165
IT	Agenzia del Farmaco	037880061, 037880097
JP	医薬品医療機器総合機構	4490034F1022
LT	Valstybinė vaistų kontrolės tarnyba	1023883, 1031086, 1031087, 1031088, 1031089, 1031090, 1031091, 1031092, 1058086, 1082389, 1082884, 1087156
NL	Z-Index G-Standaard, PRK	102415, 98426
PL	Rejestru Produktów Leczniczych	100182363, 100281987, 100385712, 100400110, 100410485, 100413590, 100413845, 100415608, 100418481, 100422904, 100434534, 100435189, 100448654
SG	Health Sciences Authority	14087P, 14868P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699514017523, 8699514590163