MERCILON

This brand name is authorized in Austria, Brazil, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, UK.

Active ingredients

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

1
UNII 81K9V7M3A3 - DESOGESTREL
 

Desogestrel is a progestogen. Like other progestogen-only pills, desogestrel is best suited for use during breast feeding and for women who may not or do not want to use oestrogens. In contrast to traditional progestogen-only pills, the contraceptive effect of desogestrel is achieved primarily by inhibition of ovulation. Other effects include increased viscosity of the cervical mucus.

 
Read more about Desogestrel
2
UNII 423D2T571U - ETHINYL ESTRADIOL
 

Ethinylestradiol is chemically and biologically identical to endogenous human oestradiol. It substitutes for the loss of estrogen production in menopausal women, and alleviates menopausal symptoms. Estrogens prevent bone loss following menopause or ovariectomy.

 
Read more about 17 alpha-Ethinylestradiol

Medicine classification

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

ATC Group Classification
G03AA09 Desogestrel and ethinylestradiol 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 G03AA09

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 527302101113413, 527303801119315, 527316010018103, 527316010018203
EE Ravimiamet 1062908, 1062919
FI Lääkealan turvallisuus- ja kehittämiskeskus 109744, 110395
FR Base de données publique des médicaments 69374160
GB Medicines & Healthcare Products Regulatory Agency 139308, 26196
HK Department of Health Drug Office 33400
IE Health Products Regulatory Authority 31402
IL מִשְׂרַד הַבְּרִיאוּת 3029, 3030
LT Valstybinė vaistų kontrolės tarnyba 1013172, 1013173, 1013174, 1064031, 1085686, 1085792
MT Medicines Authority MA031/02301, PI770/10101B, PI908/12802A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 001M93
NL Z-Index G-Standaard, PRK 78328
NZ Medicines and Medical Devices Safety Authority 3410
PL Rejestru Produktów Leczniczych 100042774, 100065440, 100266427, 100267970, 100290667, 100292703, 100314333, 100334130, 100344268, 100377055, 100417470, 100417978, 100419902, 100422040
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W68120001, W68120002, W68120003
SG Health Sciences Authority 06136P
ZA Health Products Regulatory Authority Y/18.8/78

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