MOVENTIG

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1	Naloxegol UNII 44T7335BKE - NALOXEGOL
	Naloxegol is a PEGylated derivative of the mu-opioid receptor antagonist naloxone. PEGylation reduces naloxegol’s passive permeability and also renders the compound a substrate for the P-glycoprotein transporter. Naloxegol functions as a peripherally-acting mu-opioid receptor antagonist in the gastrointestinal tract, thereby decreasing the constipating effects of opioids without impacting opioid-mediated analgesic effects on the central nervous system.
	Read more about Naloxegol

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
MOVENTIG Film-coated tablet	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
A06AH03		A Alimentary tract and metabolism → A06 Laxatives → A06A Laxatives → A06AH Peripheral opioid receptor antagonists
Discover more medicines within A06AH03

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1671241, 1671252, 1671263, 1671274, 1671285, 1778520
ES	Centro de información online de medicamentos de la AEMPS	114962001, 114962005
FI	Lääkealan turvallisuus- ja kehittämiskeskus	052280, 059012, 078038, 530118
FR	Base de données publique des médicaments	62119972, 62964361
GB	Medicines & Healthcare Products Regulatory Agency	301701, 301712
IE	Health Products Regulatory Authority	36933, 36934
IT	Agenzia del Farmaco	043793013, 043793025, 043793037, 043793049, 043793052, 043793064, 043793076, 043793088, 043793090, 043793102, 043793114
LT	Valstybinė vaistų kontrolės tarnyba	1075201, 1075202, 1075203, 1075204, 1075205, 1075206, 1075207, 1085037, 1085038, 1085039, 1086201
NL	Z-Index G-Standaard, PRK	147214, 147222
PL	Rejestru Produktów Leczniczych	100332928, 100332940
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W69023001, W69023002, W69024001, W69024002