YASMIN

This brand name is authorized in Austria, Brazil, Canada, Cyprus, Ecuador, Spain, Finland, Hong Kong, Croatia, Ireland, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, South Africa

Active ingredients

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

1 Drospirenone
UNII N295J34A25 - DROSPIRENONE

Drospirenone is a progestogen. In a therapeutic dosage, drospirenone also possesses antiandrogenic and mild antimineralocorticoid properties. It has no estrogenic, glucocorticoid and antiglucocorticoid activity. This gives drospirenone a pharmacological profile closely resembling the natural hormone progesterone.

Read about Drospirenone
2 17 alpha-Ethinylestradiol
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 about 17 alpha-Ethinylestradiol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
YASMIN Film-coated tablet Health Products Regulatory Authority (IE) 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
G03AA12 Drospirenone 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 G03AA12

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 538912050015713, 538912070018003, 538913050022403, 538915060023503
Country: CA Health Products and Food Branch Identifier(s): 02261723, 02261731
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 27.893-11-07
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 00-2881, 2000-02881IP, 23022-17-4-2008, 3303827505, 63575, 63576, 8069-1-2-11, PL00010-0571, RVG23827
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 002391, 003911, 004000
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 139812, 26464, 378893
Country: HK Department of Health Drug Office Identifier(s): 48905
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-993460030
Country: IE Health Products Regulatory Authority Identifier(s): 53010
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 4400, 4401
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1091723
Country: MT Medicines Authority Identifier(s): MA639/02801, PI1438/05301A, PI908/16401B
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 322M2002
Country: NL Z-Index G-Standaard, PRK Identifier(s): 56774
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 9899
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100031517, 100129788, 100258209, 100264760, 100266083, 100267770, 100268159, 100305222, 100324662, 100336270, 100346310, 100349745, 100351370, 100405751, 100417435, 100426730, 100446603, 100458883, 100460054
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W63899001, W63899002, W63899003, W63899004
Country: SG Health Sciences Authority Identifier(s): 12334P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699546093953, 8699546093960
Country: ZA Health Products Regulatory Authority Identifier(s): 34/18.8/0494

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