Zejula 100 mg
Zejula 100 mg is a medicine authorised by Swissmedic under authorisation number 68652. The authorisation holder is GlaxoSmithKline AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 20 January 2023 and the authorisation is limited until 19 January 2028. ATC code L01XK02 places the medicine in the group Antineoplastic agents.
| Authorisation number | 68652 |
|---|---|
| Name | Zejula 100 mg |
| Full name | Zejula 100 mg, Filmtabletten |
| Authorisation holder | GlaxoSmithKline AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | L01XK02 |
| First authorisation | 20 January 2023 |
| Authorisation validity | 19 January 2028 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Zejula 100 mg, Filmtabletten | A | 20 January 2023 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 56 | Tablette(n) | L01XK02 | 07.16.1. | A |
| 2 | 84 | Tablette(n) | L01XK02 | 07.16.1. | A |
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Frequently asked questions
Is Zejula 100 mg authorised in Switzerland?
Yes. Zejula 100 mg is authorised by Swissmedic under authorisation number 68652, data as of 01 September 2026. The authorisation is limited until 19 January 2028.
Which dispensing category does Zejula 100 mg have?
Zejula 100 mg is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.
Who is the authorisation holder of Zejula 100 mg?
The authorisation holder is GlaxoSmithKline AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.