NIQUITIN

This brand name is authorized in Austria, Brazil, Estonia, France, Ireland, Lithuania, Mexico, Netherlands, Poland, South Africa, Spain, Tunisia, UK.

Active ingredients

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

1	Nicotine UNII 6M3C89ZY6R - NICOTINE
	Nicotine, the primary alkaloid in tobacco products and a naturally occurring autonomous substance, is a nicotine receptor agonist in the peripheral and central nervous systems and has pronounced CNS and cardiovascular effects.
	Read more about Nicotine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
NIQUITIN Transdermal patch	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
N07BA01	Nicotine	N Nervous system → N07 Other nervous system drugs → N07B Drugs used in addictive disorders → N07BA Drugs used in nicotine dependence
Discover more medicines within N07BA01

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	574618120000017, 574618120000117, 574618120000217, 574619010000317, 574619010000417, 574620020000607, 574620020000707
EE	Ravimiamet	1042726, 1042737, 1042748, 1101294, 1101306, 1101317, 1277906, 1277917, 1277928, 1277939, 1535510, 1535521, 1618477, 1618488, 1638312, 1638323, 1641484, 1641495, 1641507, 1641518, 1641529, 1641530, 1641541, 1641552, 1641563, 1641574, 1642294, 1642306, 1642317, 1642328, 1642339, 1642384, 1642395, 1642407, 1642418, 1642429, 1800537, 1800548, 1800559, 1800560, 1800571, 1800582, 1800593, 1800605, 1800616, 1804182, 1804193
ES	Centro de información online de medicamentos de la AEMPS	65840, 65841, 65842, 70553, 70554, 80087
FR	Base de données publique des médicaments	61056501, 61405814, 62846498, 62854947, 64283632, 64598998, 67976232, 68284564, 68825393, 69183696, 69341566
GB	Medicines & Healthcare Products Regulatory Agency	162375, 162506, 162507, 16272, 16280, 16282, 16283, 16284, 16495, 215205, 32148, 32155, 382342, 382344, 387012, 49907, 49909, 49910
IE	Health Products Regulatory Authority	28810, 28812, 30013, 30315, 30320, 30357, 34725, 34850, 34869, 34908
LT	Valstybinė vaistų kontrolės tarnyba	1021216, 1021217, 1021218, 1021219, 1021220, 1021221, 1072650, 1072837, 1072838, 1072839, 1072840, 1075574, 1077179, 1077180, 1077181, 1077182, 1077183, 1077184, 1077185, 1077186, 1077187, 1077188, 1077189, 1077190, 1077191, 1077192, 1077193, 1077194
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	527M98
NL	Z-Index G-Standaard, PRK	70106, 70114, 70122, 84743, 90735
PL	Rejestru Produktów Leczniczych	100109952, 100112807, 100112813, 100112820, 100192752, 100208571, 100208750, 100336843, 100343949, 100343961, 100343978, 100343984, 100349780, 100424352
TN	Direction de la Pharmacie et du Médicament	1783021, 1783022, 1783023, 1783024, 1783025, 1783026, 1783027, 1783028, 1783029
ZA	Health Products Regulatory Authority	33/34/0523, 33/34/0524, 33/34/0525, A38/34/0404, A38/34/0405