YENTREVE

This brand name is authorized in Austria, Germany, Estonia, Finland, Ireland, Israel, Lithuania, Poland, United Kingdom

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 about Duloxetine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
YENTREVE Hard gastro-resistant capsule European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title 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)
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00020988, 00021539, 01463274, 01930824, 01930876, 03323666, 03324453, 05871018, 05871024, 05871047, 06734915, 06734938, 06786734, 06786740, 07049558, 07049570, 09207866, 09246116, 10201604, 12531955
Country: EE Ravimiamet Identifier(s): 1208225, 1208236, 1208247, 1208258, 1208269, 1208270, 1208281, 1285972
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 019469, 025301
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 80496, 96483
Country: IE Health Products Regulatory Authority Identifier(s): 53027, 53085
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 4891, 4892
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1029585, 1029586, 1029587, 1029588, 1029589, 1029590, 1029591, 1029592
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100127631, 100127648

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