This brand name is authorized in Austria, Estonia, Spain, Hong Kong, Croatia, Ireland, Lithuania, Malta, Poland, Romania
The drug LUTRATE contains one active pharmaceutical ingredient (API):
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1
Leuprorelin
UNII 37JNS02E7V - LEUPROLIDE ACETATE
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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. |
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 |
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 |
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: HR | Agencija za lijekove i medicinske proizvode | Identifier(s): HR-H-274164806, HR-H-434848952 |
| 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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