OBIZUR
As listed in the register: OBIZUR 500 U POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
500 U · polvo y disolvente para solución inyectable
- Prescription only
- Blood, clotting and anaemia
- Active substance
- Susoctocog
- Used in
- Blood, clotting and anaemia
- Made by
- Baxalta Innovations Gmbh
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
Mediclarum has not yet retrieved and stored the official label for this product, so none of its text is shown here. Open the official leaflet
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
NetherlandsNo exact match for this strength and form
Details
| Made by | Baxalta Innovations Gmbh |
|---|---|
| Active substance | Susoctocog |
| Used in | Blood, clotting and anaemia |
| Strength | 500 U |
| Form | polvo y disolvente para solución inyectable |
| Classification | B02BD14 · Blood, clotting and anaemia |
| Route | vía intravenosa |
| Marketed | No — authorised but not currently marketed, according to the register |
| Additional monitoring ▼ | Yes — under additional monitoring (black triangle). Report suspected side effects. |
| Name in the register | OBIZUR 500 U POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE |
| Nº Registro | 1151035 |
Source: CIMA — Centro de Información online de Medicamentos · 2026-09-30 · not reviewed by a clinician
Fuente: Agencia Española de Medicamentos y Productos Sanitarios (AEMPS), CIMA. Reuse terms: Aviso legal AEMPS.