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| Name | Leuprorelin 22.5mg powder and solvent for suspension for injection vials |
| BNF code | 0803042N0AAAEAE |
| Virtual Therapeutic Moiety | Leuprorelin |
| Abbreviated name | Leuprorelin 22.5mg inj vials |
| Basis of preferred name | rINN - Recommended International Non-proprietary |
| Prescribing status | Valid as a prescribable product |
| Sugar free | ✗ |
| Gluten free | ✗ |
| Preservative free | ✗ |
| CFC free | ✗ |
| Non-availability | Actual Products not Available |
| Non-availability status date | 1 Jan 2019 |
| Dose form | Discrete |
| Unit dose form size | 1.000 |
| Unit dose form units | vial |
| Unit dose unit of measure | vial |
| Virtual Product Ingredient | |
|---|---|
| Ingredient | Leuprorelin acetate |
| Basis of pharmaceutical strength | Based on Ingredient Substance |
| Strength value numerator | 22.500 |
| Strength value numerator unit | mg |
| Ontology Drug Form & Route | |
| Form & Route | suspensioninjection.intramuscular |
| Dose Form | |
| Formulation | Powder and solvent for suspension for injection |
| Drug Route | |
| Route | Intramuscular |
| Controlled Drug Prescribing Information | |
| Controlled Drug category | No Controlled Drug Status |
| Virtual Medicinal Product Packs | |
| Leuprorelin 22.5mg powder and solvent for suspension for injection vials 1 vial | |
dm+d data retrieved from TRUD: release NHSBSA_4.4.0_20240429000001, imported on 29th April 2024 at 05:07:25.