Pemetrexed liquid Zentiva 100 mg/10 ml
Pemetrexed liquid Zentiva 100 mg/10 ml is a medicine authorised by Swissmedic under authorisation number 69034. The authorisation holder is Helvepharm 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 July 2023 and the authorisation is limited until 19 July 2028. The export lists no ATC code for this medicine.
| Authorisation number | 69034 |
|---|---|
| Name | Pemetrexed liquid Zentiva 100 mg/10 ml |
| Full name | Pemetrexed liquid Zentiva 100 mg/10 ml, Infusionslösung |
| Authorisation holder | Helvepharm AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | not stated |
| First authorisation | 20 July 2023 |
| Authorisation validity | 19 July 2028 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Pemetrexed liquid Zentiva 100 mg/10 ml, Infusionslösung | A | 20 July 2023 |
| 2 | Pemetrexed liquid Zentiva 500 mg/50 ml, Infusionslösung | A | 20 July 2023 |
| 3 | Pemetrexed liquid Zentiva 1000 mg/100 ml, Infusionslösung | A | 20 July 2023 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| The Swissmedic export lists no pack sizes for this medicine. | |||||
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Frequently asked questions
Is Pemetrexed liquid Zentiva 100 mg/10 ml authorised in Switzerland?
Yes. Pemetrexed liquid Zentiva 100 mg/10 ml is authorised by Swissmedic under authorisation number 69034, data as of 01 September 2026. The authorisation is limited until 19 July 2028.
Which dispensing category does Pemetrexed liquid Zentiva 100 mg/10 ml have?
Pemetrexed liquid Zentiva 100 mg/10 ml 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 Pemetrexed liquid Zentiva 100 mg/10 ml?
The authorisation holder is Helvepharm 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.