Aclasta
Aclasta is a medicine authorised by Swissmedic under authorisation number 57363. The authorisation holder is Sandoz Pharmaceuticals AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 07 November 2006 and the authorisation is valid without a time limit. ATC code M05BA08 places the medicine in the group Drugs for treatment of bone diseases.
| Authorisation number | 57363 |
|---|---|
| Name | Aclasta |
| Full name | Aclasta, Infusionslösung |
| Authorisation holder | Sandoz Pharmaceuticals AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | M05BA08 |
| First authorisation | 07 November 2006 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Aclasta, Infusionslösung | B | 07 November 2006 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 1 x 100 ml | Durchstechflasche(n) | M05BA08 | 07.99.0. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Aclasta authorised in Switzerland?
Yes. Aclasta is authorised by Swissmedic under authorisation number 57363, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Aclasta have?
Aclasta is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Aclasta?
The authorisation holder is Sandoz Pharmaceuticals 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.