NUROFEN

This brand name is authorized in Austria, Cyprus, Germany, Estonia, Spain, France, Hong Kong, Croatia, Ireland, Israel, Lithuania, Malta, Nigeria, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, South Africa

Active ingredients

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

1
UNII WK2XYI10QM - IBUPROFEN
 

Ibuprofen is a propionic acid derivative NSAID that has demonstrated its efficacy by inhibition of prostaglandin synthesis. In humans ibuprofen reduces inflammatory pain, swellings and fever. Furthermore, ibuprofen reversibly inhibits platelet aggregation.

 
Read more about Ibuprofen

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 NUROFEN Coated tablet MPI, EU: SmPC Health Products Regulatory Authority (IE)
 NUROFEN DURANCE Medicated plaster 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
M01AE01 Ibuprofen M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AE Propionic acid derivatives
Discover more medicines within M01AE01
M02AA13 Ibuprofen M Musculo-skeletal system → M02 Topical products for joint and muscular pain → M02A Topical products for joint and muscular pain → M02AA Antiinflammatory preparations, non-steroids for topical use
Discover more medicines within M02AA13

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 00146519, 01170187, 02547582, 03443838, 06789419, 06789425, 07776465, 07776471, 08794436, 08794442, 08794459, 11128051, 11550548, 12741888, 13475265, 16205690, 16205709, 16516846, 16536808, 16538227, 16538233
EE Ravimiamet 1029259, 1073304, 1133569, 1133592, 1285613, 1285624, 1285646, 1285657, 1285668, 1335361, 1335372, 1335383, 1335394, 1335406, 1335417, 1335428, 1335439, 1335440, 1335451, 1335462, 1335473, 1386479, 1386604, 1386615, 1386626, 1386671, 1386682, 1386693, 1386705, 1607521, 1637096, 1637108, 1683435, 1683446, 1683457, 1683468, 1683479, 1683480, 1683491, 1683503, 1683514, 1683525, 1683536, 1683547, 1683558, 1683569, 1683570, 1683581, 1769654, 1769665, 1769676, 1769687, 1769698, 1836198, 1836222
ES Centro de información online de medicamentos de la AEMPS 67968, 68517, 78466, 78530, 82519
FR Base de données publique des médicaments 60305960, 60830246, 61471853, 63005402, 64911902, 65750786, 67510932, 68354856, 69457752, 69543863
GB Medicines & Healthcare Products Regulatory Agency 102397, 115076, 115077, 119346, 119347, 119348, 119350, 139407, 139426, 14595, 146007, 14601, 14603, 14605, 14607, 14608, 14609, 147410, 215242, 22565, 236497, 236499, 313932, 313946, 313950, 313953, 313958, 323202, 323909, 357487, 357488, 38692, 386928, 386930, 46040, 46057, 80617, 91644, 91645, 91647
HK Department of Health Drug Office 51501, 58322, 64198, 64199
HR Agencija za lijekove i medicinske proizvode HR-H-023698858, HR-H-140153836, HR-H-151406116, HR-H-534899919, HR-H-756646540, HR-H-821340280, HR-H-846940596, HR-H-934065674, HR-H-987481558
IL מִשְׂרַד הַבְּרִיאוּת 182, 3945, 3999, 5080, 5081, 5087, 5197, 5198, 5225, 5226, 5250, 5262, 5263, 5391, 5409, 5410, 5464, 5494, 5497
LT Valstybinė vaistų kontrolės tarnyba 1011544, 1015741, 1015742, 1030746, 1030747, 1035012, 1035013, 1058611, 1058612, 1058613, 1058614, 1058615, 1058616, 1059887, 1072175, 1072190, 1076350, 1081794, 1081795, 1081796, 1081797, 1081798, 1081799, 1081800, 1081801, 1081802, 1081803, 1081804, 1081805, 1081806, 1081807, 1081808, 1091577, 1091578
MT Medicines Authority AA1228/01401, AA908/08004, MA1447/00102, MA1447/00103, MA1447/00402, MA190/00402, PI1438/09801A, PI908/08001A
NG Registered Drug Product Database A4-5985, B4-4444, B4-5558
Switch country to NG in order to find specific presentations of NUROFEN
NL Z-Index G-Standaard 14132265, 15092356
NL Z-Index G-Standaard, PRK 17760, 197998, 27251, 27278, 47872, 54801, 59072, 67962, 69248
NZ Medicines and Medical Devices Safety Authority 11233, 11234, 11602, 11604, 11606, 12185, 12367, 12370, 12823, 12824, 12825, 12826, 12827, 13266, 13267, 14111, 14156, 14859, 14860, 17637, 19916, 20766, 8574, 991, 9922
PL Rejestru Produktów Leczniczych 100090945, 100094877, 100096497, 100114806, 100161987, 100162900, 100165459, 100172755, 100181820, 100191103, 100198424, 100216464, 100229372, 100241686, 100241692, 100274987, 100307830, 100335677, 100335683, 100338836, 100339899, 100343323, 100356834, 100367230, 100392043, 100393290, 100393462, 100397661, 100400512, 100404591, 100411510, 100418742, 100418765, 100419517, 100429941, 100429993, 100435522, 100438816, 100444828, 100446951, 100464710
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W65692001, W65692002, W65692003, W65692004, W65692005, W65692006, W65692007, W65943002, W65943003, W66067001, W66067002, W66067003, W66067004, W66067005, W66067006, W66068002, W66069001, W66069002, W66069003, W66069004, W66069005, W66069006, W66069007, W66070001, W66070002, W66070003, W66070004, W66070005, W66072001, W66073001, W66073002, W66073003, W66074001, W66083001, W66083002, W66083003, W66083004, W66083005, W66084001, W66084002, W66084003, W66084004, W66084005, W66085001, W66085002, W66085003, W66085004, W66085005, W66085006, W66085007, W66085008, W66085009, W66088001, W66088002, W66088003, W66088004, W66088005, W66088006, W66088007, W66088008, W66088009, W66088010, W66088011, W66088012, W66094001, W66094002, W66094003, W66094004, W66094005, W66094006, W66094007, W66094008, W66094009, W66094010, W66094011, W66094012, W66094013, W66094014, W66094015, W66094016, W66095002, W66095004, W66095006, W67838001, W67838002, W67838003, W67838004, W69383001
SG Health Sciences Authority 09488P, 10923P, 10924P, 11879P, 11880P, 14366P, 14367P, 14561P, 14562P, 14587P, 14958P, 15309P
TR İlaç ve Tıbbi Cihaz Kurumu 8690570120028, 8690570120035, 8690570120042, 8690570700022
ZA Health Products Regulatory Authority 31/2.7/0466, 35/2.7/0077, 36/2.7/0029, 36/2.7/0184, 36/3.1/0433, 44/2.7/0386, 45/2.7/0781, 47/2.7/0289, 49/2.7/0178, 49/2.7/0179, A40/2.7/0092, S/2.7/123, W/2.7/142, W/2.7/49

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