Allergovit Betula Kombipackung
Allergovit Betula Kombipackung is a medicine authorised by Swissmedic under authorisation number 60642. The authorisation holder is Dermapharm AG. The medicinal product code is Allergen: therapeutic 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 30 August 2010 and the authorisation is valid without a time limit. ATC code V01AA places the medicine in the group Allergens.
| Authorisation number | 60642 |
|---|---|
| Name | Allergovit Betula Kombipackung |
| Full name | Allergovit Betula Kombipackung, Injektionssuspension |
| Authorisation holder | Dermapharm AG |
| Medicinal product code | Allergen: therapeutic |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | V01AA |
| First authorisation | 30 August 2010 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Allergovit Betula Kombipackung, Injektionssuspension | A | 30 August 2010 |
| 2 | Allergovit Betula Stärke B, Injektionssuspension | A | 30 August 2010 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 2 x 3ml | Durchstechflasche(n) | V01AA | 07.13.3. | A |
| 2 | 1 x 3 ml | Durchstechflasche(n) | V01AA | 07.13.3. | A |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Allergovit Betula Kombipackung authorised in Switzerland?
Yes. Allergovit Betula Kombipackung is authorised by Swissmedic under authorisation number 60642, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Allergovit Betula Kombipackung have?
Allergovit Betula Kombipackung 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 Allergovit Betula Kombipackung?
The authorisation holder is Dermapharm 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.