ZOELY

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

Active ingredients

The drug ZOELY contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 83J78V5W05 - NOMEGESTROL ACETATE
 
Read more about Nomegestrol
2
UNII 4TI98Z838E - ESTRADIOL
 

Estradiol, is chemically and biologically identical to endogenous human estradiol. It substitutes for the loss of oestrogen production in menopausal women, and alleviates menopausal symptoms. Oestrogens prevent bone loss following menopause or ovariectomy.

 
Read more about Estradiol

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZOELY 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
G03AA14 Nomegestrol and estradiol G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AA Progestogens and estrogens, fixed combinations
Discover more medicines within G03AA14

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 1549863, 1549874, 1598733, 1598777
ES Centro de información online de medicamentos de la AEMPS 11690001, 11690002
FI Lääkealan turvallisuus- ja kehittämiskeskus 034113, 199259
FR Base de données publique des médicaments 61335127
GB Medicines & Healthcare Products Regulatory Agency 223117
IE Health Products Regulatory Authority 33330
IL מִשְׂרַד הַבְּרִיאוּת 7319, 7320
IT Agenzia del Farmaco 041400019, 041400021, 041400033, 041400045, 046328011, 046328023, 048519019, 049590019, 050016017
LT Valstybinė vaistų kontrolės tarnyba 1061636, 1061637, 1068576, 1068577
MX Comisión Federal para la Protección contra Riesgos Sanitarios 238M2014
NL Z-Index G-Standaard, PRK 101567
PL Rejestru Produktów Leczniczych 100245804
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W65719001
ZA Health Products Regulatory Authority 45/18.8/0064

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