CERAZETTE

This brand name is authorized in Austria, Brazil, Ecuador, Estonia, Finland, France, Ireland, Israel, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, South Africa, Turkey, UK.

Active ingredients

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

1	Desogestrel 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

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
CERAZETTE Film-coated 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
G03AC09	Desogestrel	G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AC Progestogens
Discover more medicines within G03AC09

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	527300201110312, 527313010009603
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	26.224-03-05
EE	Ravimiamet	1010675, 1063303, 1063314, 1589519, 1861871, 1861882, 1861893
FI	Lääkealan turvallisuus- ja kehittämiskeskus	518332
FR	Base de données publique des médicaments	61452187
GB	Medicines & Healthcare Products Regulatory Agency	34116
IE	Health Products Regulatory Authority	65410
IL	מִשְׂרַד הַבְּרִיאוּת	4758, 4759
LT	Valstybinė vaistų kontrolės tarnyba	1014148, 1014149, 1067338, 1067339, 1087556
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	331M99
NL	Z-Index G-Standaard, PRK	56111
NZ	Medicines and Medical Devices Safety Authority	8026
PL	Rejestru Produktów Leczniczych	100106907, 100265920, 100269012, 100300207, 100304501, 100309125, 100335016, 100335281, 100342447, 100342683, 100361870, 100396839, 100420176, 100432280, 100432788, 100447034, 100456995
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W68119001, W68119002, W68119003
TR	İlaç ve Tıbbi Cihaz Kurumu	8683280337046
ZA	Health Products Regulatory Authority	46/34/0891