LUTRATE

This brand name is authorized in Austria, Estonia, Spain, Hong Kong, Ireland, Lithuania, Malta, Poland, Romania

Active ingredients

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

1 Leuprorelin
UNII 37JNS02E7V - LEUPROLIDE ACETATE

Leuprorelin is inactive when given orally due to poor membrane permeability and an almost complete inactivation by intestinal proteolytic enzymes. Leuprorelin has potent LHRH agonist properties when given during short-term and intermittent therapy, however, when administered in a continuous, nonpulsatile manner, LHRH analogs induce inhibition of gonadotropin secretion and suppression of testicular steroidogenesis.

Read about Leuprorelin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
LUTRATE DEPOT Powder and solvent for prolonged-release suspension for injection 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
L02AE02 Leuprorelin L Antineoplastic and immunomodulating agents → L02 Endocrine therapy → L02A Hormones and related agents → L02AE Gonadotropin releasing hormone analogues
Discover more medicines within L02AE02

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): 1544532, 1645758
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 80000, 83377
Country: HK Department of Health Drug Office Identifier(s): 63523, 65851
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1063139, 1073229
Country: MT Medicines Authority Identifier(s): AA1173/07601, AA565/42901
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100298462, 100344564
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W67840001

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