NEOCLARITYN

This brand name is authorized in Austria, Estonia, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

The drug NEOCLARITYN 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 about Desloratadine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
Neoclarityn 5 mg film-coated tablets	Medicines & Healthcare Products Regulatory Agency (GB)	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
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)
Country: EE	Ravimiamet	Identifier(s): 1197941, 1197952, 1197963, 1197974, 1197985, 1197996, 1198009, 1198010, 1198021, 1198032, 1198043, 1198054, 1198065, 1198155, 1198166, 1198177, 1198188, 1198199, 1198201, 1198212, 1198223, 1198234, 1198245, 1198256, 1198267, 1198278, 1368222, 1368233, 1368244, 1368255, 1368266, 1368277, 1368288, 1368299, 1368301, 1368312, 1368323, 1368334, 1368345, 1368356, 1368367, 1368378, 1368389, 1368390, 1368402, 1368413, 1368424, 1368435, 1368446, 1368457, 1368468, 1368479, 1368480, 1368491, 1368503, 1368514, 1368525, 1368536
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 139363, 160981, 162994, 21632
Country: IE	Health Products Regulatory Authority	Identifier(s): 35705, 35821, 35841, 35847, 35853, 35860
Country: IT	Agenzia del Farmaco	Identifier(s): 035204015, 035204027, 035204039, 035204041, 035204054, 035204066, 035204078, 035204080, 035204092, 035204104, 035204116, 035204128, 035204130, 035204142, 035204155, 035204167, 035204179, 035204181, 035204193, 035204205, 035204217
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1029477, 1029478, 1029479, 1029480, 1029481, 1029482, 1029483, 1029484, 1029485, 1029486, 1029487, 1029488, 1029489, 1029490, 1029491, 1029492, 1029493, 1029494, 1029495, 1029496, 1029497, 1029498, 1029507, 1029508, 1029509, 1029510, 1029511, 1029512, 1029513, 1029514, 1029515, 1029516, 1029517, 1029518, 1029519, 1029520, 1029521, 1029522, 1029523, 1029524, 1029525, 1029526, 1029527, 1029528, 1029529, 1029530
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 59021
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100125945, 100233570, 100233592, 100233617
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W51594001, W51594002, W51594003, W51594004, W51594005, W51594006, W51594007, W51594008, W51594009, W51594010, W51594011, W51594012, W51594013, W51596001, W51596002, W51596003, W51596004, W51596005, W51596006, W51596007, W51596008, W51596009, W51596010, W51596011, W51596012, W51596013, W52640001, W52640002, W52640003, W52640004, W52640005, W52640006, W52640007, W52640008, W52640009, W52640010, W52640011, W52640012, W52641001, W52641002, W52641003, W52641004, W52641005, W52641006, W52641007, W52641008, W52641009, W52641010, W52641011, W52641012, W52642001, W52642002, W52642003, W52642004, W52642005, W52642006, W52642007, W52642008