CYCLOGEST

This brand name is authorized in Austria, Croatia, Cyprus, Finland, Hong Kong SAR China, Malta, Netherlands, Nigeria, Poland, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1
UNII 4G7DS2Q64Y - PROGESTERONE
 

Progesterone is a natural progestogen, the main hormone of the corpus luteum and the placenta. It acts on the endometrium by converting the proliferating phase to the secretory phase.
 
Read more about Progesterone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CYCLOGEST Off-white pessaries 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
G03DA04 Progesterone G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03D Progestogens → G03DA Pregnen (4) derivatives
Discover more medicines within G03DA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
ES Centro de información online de medicamentos de la AEMPS 82250
FI Lääkealan turvallisuus- ja kehittämiskeskus 377577
GB Medicines & Healthcare Products Regulatory Agency 24753, 39132
HK Department of Health Drug Office 31619, 64360
HR Agencija za lijekove i medicinske proizvode HR-H-296223562
MT Medicines Authority MA1031/00801, PI1438/01801A, PI908/20901A
NG Registered Drug Product Database A4-0236
Switch country to Nigeria in order to find specific presentations of CYCLOGEST
NL Z-Index G-Standaard, PRK 201375
PL Rejestru Produktów Leczniczych 100364839
SG Health Sciences Authority 03626P
TN Direction de la Pharmacie et du Médicament 10633011, 10633012, 22493011, 22493012
TR İlaç ve Tıbbi Cihaz Kurumu 8699708900280, 8699708900297
ZA Health Products Regulatory Authority Z/21.8.2/294

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