ESTROFEM

This brand name is authorized in Austria, Estonia, Finland, France, Hong Kong, Croatia, Ireland, Israel, Lithuania, Netherlands, New Zealand, Poland, Singapore, Turkey, South Africa

Active ingredients

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

1 Estradiol 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 about Estradiol

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ESTROFEM 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
G03CA03	Estradiol	G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03C Estrogens → G03CA Natural and semisynthetic estrogens, plain
Discover more medicines within G03CA03

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EE	Ravimiamet	Identifier(s): 1030431, 1030442, 1684111, 1829752, 1848382, 1848393
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 487512, 494666
Country: FR	Base de données publique des médicaments	Identifier(s): 64183183, 66189217
Country: HK	Department of Health Drug Office	Identifier(s): 34267, 42910
Country: IE	Health Products Regulatory Authority	Identifier(s): 23655
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 2694, 3867
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1000738, 1004206, 1085574, 1085575, 1088294, 1088358, 1088359, 1088375, 1091298, 1092141
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 78123
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 5205, 5206
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100022820, 100096238
Country: SG	Health Sciences Authority	Identifier(s): 06009P, 09922P
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699676090266
Country: ZA	Health Products Regulatory Authority	Identifier(s): 34/21.8.1/0159, J/21.8.1/214