LENZETTO

This brand name is authorized in Ecuador, Estonia, Spain, Finland, Croatia, Ireland, Lithuania, Malta, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Estradiol
UNII CXY7B3Q98Z - ESTRADIOL HEMIHYDRATE

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  
LENZETTO Transdermal spray, solution Medicines & Healthcare Products Regulatory Agency (GB) 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: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 2781-MEE-0517
Country: EE Ravimiamet Identifier(s): 1632169, 1715611, 1849798
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 80608
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 053018, 396436
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 382693, 382698
Country: IE Health Products Regulatory Authority Identifier(s): 78085
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1072022, 1080059
Country: MT Medicines Authority Identifier(s): MA1031/00101
Country: NL Z-Index G-Standaard, PRK Identifier(s): 167266
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100347999
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W62058002, W62058003

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