MIFEGYNE

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Netherlands, New Zealand, Romania, Singapore, South Africa, Spain, Tunisia, UK.

Active ingredients

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

1
UNII 320T6RNW1F - MIFEPRISTONE
 

Mifepristone is a synthetic steroid with an antiprogestational action as a result of competition with progesterone at the progesterone receptors.

 
Read more about Mifepristone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 MIFEGYNE Tablet 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
G03XB01 Mifepristone G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03X Other sex hormones and modulators of the genital system → G03XB Antiprogestogens
Discover more medicines within G03XB01

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 1082786, 1428016, 1537107, 1537118, 1833825, 1833836, 1833847, 1833858, 1861837, 1861859, 1861860
ES Centro de información online de medicamentos de la AEMPS 62728
FI Lääkealan turvallisuus- ja kehittämiskeskus 572020
FR Base de données publique des médicaments 62681445, 66422290
GB Medicines & Healthcare Products Regulatory Agency 48310
HK Department of Health Drug Office 62757
HR Agencija za lijekove i medicinske proizvode HR-H-135441123
IL מִשְׂרַד הַבְּרִיאוּת 7310
NL Z-Index G-Standaard, PRK 59293
NZ Medicines and Medical Devices Safety Authority 9791
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W53133001, W53133002, W53133003, W53133004, W61401001, W61401002, W61401003, W61401004
SG Health Sciences Authority 15583P
TN Direction de la Pharmacie et du Médicament 4303011H
ZA Health Products Regulatory Authority 34/21.12/0328

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