KESIMPTA
As listed in the register: KESIMPTA 20 mg, solution injectable en stylo prérempli
20 mg · solution injectable
- Prescription only
- Active substance
- Ofatumumab
- Made by
- NOVARTIS EUROPHARM (IRLANDE)
- 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
United StatesNo exact match for this strength and form
European UnionNo exact match for this strength and form
Spain2 matching products
CanadaNo exact match for this strength and form
Netherlands2 matching products
Details
| Made by | NOVARTIS EUROPHARM (IRLANDE) |
|---|---|
| Active substance | Ofatumumab |
| Strength | 20 mg |
| Form | solution injectable |
| Route | sous-cutanée |
| Dispensing (as stated by the register) | prescription réservée aux spécialistes et services NEUROLOGIE · médicament nécessitant une surveillance particulière pendant le traitement · liste I |
| Marketed | Yes, according to the register |
| Authorisation procedure | Procédure centralisée |
| EU number | EU/1/21/1532 |
| Name in the register | KESIMPTA 20 mg, solution injectable en stylo prérempli |
| Packs | 1 stylo prérempli en verre de 0,4 ml |
| CIS | 60690011 |
| CIP13 | 3400930226971 |
Source: Base de données publique des médicaments · 2026-09-30 · not reviewed by a clinician
Source : Base de données publique des médicaments (ANSM / Ministère de la Santé), sous Licence Ouverte. Reuse terms: Licence Ouverte / Open Licence (Etalab).