Neulasta
Neulasta is a medicine authorised by Swissmedic under authorisation number 56326. The authorisation holder is Amgen Switzerland AG. The medicinal product code is Biotechnological 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 01 September 2003 and the authorisation is valid without a time limit. ATC code L03AA13 places the medicine in the group Immunostimulants.
| Authorisation number | 56326 |
|---|---|
| Name | Neulasta |
| Full name | Neulasta, Injektionslösung in einer Fertigspritze |
| Authorisation holder | Amgen Switzerland AG |
| Medicinal product code | Biotechnological medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | L03AA13 |
| First authorisation | 01 September 2003 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Neulasta, Injektionslösung in einer Fertigspritze | A | 01 September 2003 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 4 | 1 | Spritze(n) | L03AA13 | 06.07.3. | A |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Neulasta authorised in Switzerland?
Yes. Neulasta is authorised by Swissmedic under authorisation number 56326, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Neulasta have?
Neulasta 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 Neulasta?
The authorisation holder is Amgen Switzerland 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.