ESTRADOT

This brand name is authorized in Australia, Austria, Brazil, Canada, Croatia, Estonia, Finland, Ireland, New Zealand, South Africa, Spain, UK.

Active ingredients

The drug ESTRADOT 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
ESTRADOT Transdermal patch	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
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)
AU	Pharmaceutical Benefits Scheme	8761D, 8762E, 8763F, 8764G, 8765H
BR	Câmara de Regulação do Mercado de Medicamentos	526505801170411, 526505802177411, 526505803173418
CA	Health Products and Food Branch	02243999, 02244000, 02244001, 02244002, 02245676
EE	Ravimiamet	1476222
ES	Centro de información online de medicamentos de la AEMPS	64704, 64705, 64707, 66103
FI	Lääkealan turvallisuus- ja kehittämiskeskus	005589, 005623, 005634, 005650, 018365
GB	Medicines & Healthcare Products Regulatory Agency	142282, 142284, 142286, 142288, 90450, 90452, 90454, 90456, 90458
HR	Agencija za lijekove i medicinske proizvode	HR-H-207838847, HR-H-259673389, HR-H-660461417
IE	Health Products Regulatory Authority	47415, 48323, 57226, 68314
NZ	Medicines and Medical Devices Safety Authority	10498, 10499, 10500, 10501, 10955
ZA	Health Products Regulatory Authority	37/21.8.1/0216, 37/21.8.1/0217, 37/21.8.1/0218, 37/21.8.1/0493