MUSE

This brand name is authorized in Austria, Canada, Estonia, Spain, Finland, Ireland, Lithuania, Netherlands, United Kingdom, United States

Active ingredients

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

1 Alprostadil
UNII F5TD010360 - ALPROSTADIL

Alprostadil is chemically identical to prostaglandin E1, the actions of which include vasodilatation of blood vessels in the erectile tissues of the corpora cavernosa and increase in cavernosal artery blood flow, causing penile rigidity.

Read about Alprostadil

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
MUSE Urethral Stick Medicines & Healthcare Products Regulatory Agency (GB) 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
G04BE01 Alprostadil G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics → G04BE Drugs used in erectile dysfunction
Discover more medicines within G04BE01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02238593, 02238594, 02238595
Country: EE Ravimiamet Identifier(s): 1146237, 1146248, 1146259, 1146260, 1146271, 1146282, 1815173, 1825309, 1882436, 1888511
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 62697, 62698
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 004360, 004369, 004385, 004391
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 28202, 28203, 28204, 28206
Country: IE Health Products Regulatory Authority Identifier(s): 32411, 32492
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1016113, 1016114, 1016115, 1016116, 1016117, 1016118
Country: NL Z-Index G-Standaard, PRK Identifier(s): 52256, 52264
Country: US FDA, National Drug Code Identifier(s): 0037-8110, 0037-8120, 0037-8130, 0037-8140

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