STRATTERA

This brand name is authorized in United States. It is also authorized in Australia, Austria, Canada, Cyprus, Ecuador, Estonia, Finland, Germany, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1	Atomoxetine UNII 57WVB6I2W0 - ATOMOXETINE HYDROCHLORIDE
	Atomoxetine is a highly selective and potent inhibitor of the pre-synaptic noradrenaline transporter, its presumed mechanism of action, without directly affecting the serotonin or dopamine transporters.
	Read more about Atomoxetine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
STRATTERA Capsule, hard	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group		Classification
N06BA09	Atomoxetine	N Nervous system → N06 Psychoanaleptics → N06B Psychostimulants, agents used for ADHD and nootropics → N06BA Centrally acting sympathomimetics
Discover more medicines within N06BA09

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	9092M, 9093N, 9094P, 9095Q, 9096R, 9289X, 9290Y
CA	Health Products and Food Branch	02262800, 02262819, 02262827, 02262835, 02262843, 02279347, 02279355
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	01137008, 03881484, 03881490, 04192769, 04192775, 04192781, 04192798, 04192806, 04192812, 04192829, 04192858, 04192870, 07176392, 10180026, 10304764, 10304770, 10325938, 10325944, 10355537, 10355543
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	26.133-01-05, 26.831-01-06, 27.084-06-06, 27.208-08-06, 27.322-10-06
EE	Ravimiamet	1190685, 1190696, 1190708, 1190719, 1190720, 1190731, 1190742, 1190753, 1190764, 1190775, 1190786, 1190797, 1190809, 1190810, 1190821, 1190832, 1190843, 1190854, 1190865, 1190876, 1299595, 1299607, 1299618, 1299629, 1299630, 1299641, 1299652, 1299663, 1635094, 1874886
ES	Centro de información online de medicamentos de la AEMPS	67656, 67657, 67659, 67660, 67661, 70123, 70124, 79268
FI	Lääkealan turvallisuus- ja kehittämiskeskus	019800, 019811, 019822, 019833, 019849, 019857, 019868, 019882, 019904, 146473, 514840
GB	Medicines & Healthcare Products Regulatory Agency	138688, 217046, 301686, 76437, 76439, 76495, 76496, 76500, 76501, 76505, 76506, 76509
HK	Department of Health Drug Office	53425, 53426, 53427, 53428, 53429, 61959
IE	Health Products Regulatory Authority	47205, 47206, 47208, 47229, 47236, 47263, 47288, 47297
IL	מִשְׂרַד הַבְּרִיאוּת	7947, 7948, 7949, 7950, 7951, 7952, 7953, 8358
JP	医薬品医療機器総合機構	1179050M1023, 1179050M2020, 1179050M3026, 1179050M4022, 1179050S1022
LT	Valstybinė vaistų kontrolės tarnyba	1020642, 1020643, 1020644, 1020645, 1020646, 1020647, 1020648, 1020649, 1020650, 1020651, 1020652, 1020653, 1020654, 1020655, 1020656, 1020657, 1020658, 1020659, 1020660, 1020661, 1025661, 1025662, 1035603, 1035604, 1035605, 1035606, 1035607, 1035608, 1072338, 1076136
MT	Medicines Authority	MA637/00101, MA637/00102, MA637/00103, MA637/00104, MA637/00105, MA637/00106, MA637/00107
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	220M2003
NL	Z-Index G-Standaard, PRK	105309, 76708, 76716, 76724, 76732, 76740, 89494
NZ	Medicines and Medical Devices Safety Authority	10733, 10734, 10735, 10736, 10737, 10738, 13378, 13379
PL	Rejestru Produktów Leczniczych	100159074, 100159097, 100159105, 100159111, 100159128
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W65180001, W65180002, W65180003, W65180004, W65181001, W65181002, W65181003, W65181004, W65182001, W65182002, W65183001, W65183002, W65183003, W65183004, W65184001, W65184002, W65184003, W65184004, W65185001, W65185002, W65185003, W65185004, W65186001, W65186002, W65186003, W65186004, W65187001, W65187002, W65187003, W65187004
SG	Health Sciences Authority	13071P, 13072P, 13073P, 13074P, 13075P
TN	Direction de la Pharmacie et du Médicament	8483011, 8483012, 8483013, 8483014, 8483015
TR	İlaç ve Tıbbi Cihaz Kurumu	8699673150192, 8699673150215, 8699673150239, 8699673150253, 8699673150277, 8699673150284, 8699673150291, 8699673156019
US	FDA, National Drug Code	0002-3227, 0002-3228, 0002-3229, 0002-3238, 0002-3239, 0002-3250, 0002-3251
ZA	Health Products Regulatory Authority	42/1.2/0789, A38/1.2/0520, A38/1.2/0521, A38/1.2/0522, A38/1.2/0523, A38/1.2/0524