NEUPRO

This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Italy, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, UK.

Active ingredients

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

1
UNII 87T4T8BO2E - ROTIGOTINE
 

Rotigotine is a non-ergolinic dopamine agonist for the treatment of signs and symptoms of Parkinson’s disease and Restless Legs Syndrome.

 
Read more about Rotigotine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 NEUPRO 4mg/24h, 6mg/24h, 8mg/24h Transdermal patch MPI, EU: SmPC European Medicines Agency (EU)
 NEUPRO 1mg/24h, 3mg/24h Transdermal patch MPI, EU: SmPC European Medicines Agency (EU)
 NEUPRO 2mg/24h Transdermal patch 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
N04BC09 Rotigotine N Nervous system → N04 Anti-parkinson drugs → N04B Dopaminergic agents → N04BC Dopamine agonists
Discover more medicines within N04BC09

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 11140H, 2384L, 2385M, 2410W
BR Câmara de Regulação do Mercado de Medicamentos 525215020020402, 525215020020502, 525215020020602, 525215020020702, 525215080020802, 525215080020902, 525215080021002
CA Health Products and Food Branch 02403897, 02403900, 02403919, 02403927, 02403935, 02403943
EE Ravimiamet 1245765, 1245776, 1245787, 1245798, 1245800, 1245811, 1245822, 1245833, 1245844, 1245855, 1245866, 1245877, 1245888, 1369111, 1369122, 1369133, 1369144, 1369155, 1369166, 1369177, 1369188, 1369199, 1369201, 1369212, 1369223, 1369234, 1369245, 1369256, 1369267, 1369278, 1369289, 1369302, 1369313, 1369324, 1369335, 1369346, 1369357, 1426261, 1426272, 1426283, 1426294, 1426306, 1426317, 1426328, 1426339, 1426340, 1426351, 1426362, 1426373, 1426384, 1426395, 1426407, 1426418, 1426429, 1426430, 1753972, 1753983, 1753994, 1754007, 1754018, 1754029
ES Centro de información online de medicamentos de la AEMPS 05331002, 05331005, 05331008, 05331011, 05331040, 05331049
FI Lääkealan turvallisuus- ja kehittämiskeskus 054914, 054923, 054942, 055332, 055351, 055360, 055369
FR Base de données publique des médicaments 60200500, 61578613, 66662951, 69741731
GB Medicines & Healthcare Products Regulatory Agency 101277, 101279, 101284, 101285, 101290, 101291, 101296, 101297, 166650, 166693, 180530, 180531, 180532, 180533, 200347, 200349, 368168, 368172, 368176, 368178, 375202, 375204, 375205, 375207, 375208, 375230, 376938, 376942, 376945, 376947, 381546, 381548, 381550, 381552
HK Department of Health Drug Office 55444, 55445, 55446, 55447
IE Health Products Regulatory Authority 13168, 19300, 19347, 19369, 37910, 37911, 37912, 37913, 37915, 37942, 37957, 37998, 44506, 44528, 44529, 44560, 44561, 44562, 44563, 44569
IT Agenzia del Farmaco 037152016, 037152028, 037152030, 037152042, 037152055, 037152067, 037152079, 037152081, 037152093, 037152105, 037152117, 037152129, 037152131, 037152143, 037152156, 037152168, 037152170, 037152182, 037152194, 037152206, 037152218, 037152220, 037152232, 037152244, 037152257, 037152269, 037152271, 037152283, 037152295, 037152307, 037152319, 037152321, 037152333, 037152345, 037152358
JP 医薬品医療機器総合機構 1169700S1025, 1169700S2021, 1169700S3028, 1169700S4024, 1169700S5020
LT Valstybinė vaistų kontrolės tarnyba 1029544, 1029545, 1029546, 1029549, 1029552, 1029554, 1029555, 1029558, 1029561, 1029563, 1029564, 1029567, 1029570, 1029572, 1029573, 1029576, 1029579, 1034040, 1034042, 1034043, 1034046, 1034049, 1034051, 1034052, 1034055, 1084257, 1084258, 1084259, 1084260, 1084261, 1084262
NL Z-Index G-Standaard, PRK 119091, 119105, 86002, 86010, 86029, 86037
PL Rejestru Produktów Leczniczych 100161183, 100161190, 100161208, 100161214, 100161243, 100199458, 100199464
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64036003, W64037003, W64038003, W64039003
SG Health Sciences Authority 14233P, 14234P, 14235P, 14236P
US FDA, National Drug Code 50474-801, 50474-802, 50474-803, 50474-804, 50474-805, 50474-806

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