ESTROFEM

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

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 more about Estradiol

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
ESTROFEM Film-coated tablet	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group		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)
EE	Ravimiamet	1030431, 1030442, 1684111, 1829752, 1848382, 1848393
FI	Lääkealan turvallisuus- ja kehittämiskeskus	487512, 494666
FR	Base de données publique des médicaments	64183183, 66189217
HK	Department of Health Drug Office	34267, 42910
HR	Agencija za lijekove i medicinske proizvode	HR-H-704743488, HR-H-810329935
IE	Health Products Regulatory Authority	23655
IL	מִשְׂרַד הַבְּרִיאוּת	2694, 3867
LT	Valstybinė vaistų kontrolės tarnyba	1000738, 1004206, 1085574, 1085575, 1088294, 1088358, 1088359, 1088375, 1091298, 1092141
NL	Z-Index G-Standaard, PRK	78123
NZ	Medicines and Medical Devices Safety Authority	5205, 5206
PL	Rejestru Produktów Leczniczych	100022820, 100096238
SG	Health Sciences Authority	06009P, 09922P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699676090266
ZA	Health Products Regulatory Authority	34/21.8.1/0159, J/21.8.1/214