YENTREVE

This brand name is authorized in Austria, Croatia, Estonia, Finland, France, Germany, Ireland, Israel, Italy, Lithuania, Poland, UK.

Active ingredients

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

1	Duloxetine UNII 9044SC542W - DULOXETINE HYDROCHLORIDE
	Duloxetine is a combined serotonin (5-HT) and noradrenaline (NA) reuptake inhibitor. It weakly inhibits dopamine reuptake with no significant affinity for histaminergic, dopaminergic, cholinergic and adrenergic receptors.
	Read more about Duloxetine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
YENTREVE Hard gastro-resistant capsule	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
N06AX21	Duloxetine	N Nervous system → N06 Psychoanaleptics → N06A Antidepressants → N06AX Other antidepressants
Discover more medicines within N06AX21

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	00020988, 00021539, 01463274, 01930824, 01930876, 03323666, 03324453, 05871018, 05871024, 05871047, 06734915, 06734938, 06786734, 06786740, 07049558, 07049570, 09207866, 09246116, 10201604, 12531955
EE	Ravimiamet	1208225, 1208236, 1208247, 1208258, 1208269, 1208270, 1208281, 1285972
FI	Lääkealan turvallisuus- ja kehittämiskeskus	019469, 025301
FR	Base de données publique des médicaments	64313246, 66056779
GB	Medicines & Healthcare Products Regulatory Agency	80496, 96483
IE	Health Products Regulatory Authority	53027, 53085
IL	מִשְׂרַד הַבְּרִיאוּת	4891, 4892
IT	Agenzia del Farmaco	036581015, 036581027, 036581039, 036581041, 036581054, 036581066, 036581078
LT	Valstybinė vaistų kontrolės tarnyba	1029585, 1029586, 1029587, 1029588, 1029589, 1029590, 1029591, 1029592
PL	Rejestru Produktów Leczniczych	100127631, 100127648