Allergovit Plantago Kombipackung
Allergovit Plantago Kombipackung is a medicine authorised by Swissmedic under authorisation number 60632. 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 | 60632 |
|---|---|
| Name | Allergovit Plantago Kombipackung |
| Full name | Allergovit Plantago 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 Plantago Kombipackung, Injektionssuspension | A | 30 August 2010 |
| 2 | Allergovit Plantago Stärke B, Injektionssuspension | A | 30 August 2010 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 2 x 3 ml | 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 Plantago Kombipackung authorised in Switzerland?
Yes. Allergovit Plantago Kombipackung is authorised by Swissmedic under authorisation number 60632, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Allergovit Plantago Kombipackung have?
Allergovit Plantago 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 Plantago 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.