Allergovit Alnus/Corylus Kombipackung

Allergovit Alnus/Corylus Kombipackung is a medicine authorised by Swissmedic under authorisation number 60624. 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.

  • Dispensing category A
  • Authorisation number 60624
  • ATC V01AA
  • Allergen: therapeutic
Authorisation data
Authorisation number60624
NameAllergovit Alnus/Corylus Kombipackung
Full nameAllergovit Alnus/Corylus Kombipackung, Injektionssuspension
Authorisation holderDermapharm AG
Medicinal product codeAllergen: therapeutic
Dispensing categoryA · Prescription, not repeatable
ATC codeV01AA
First authorisation30 August 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Allergovit Alnus/Corylus Kombipackung, InjektionssuspensionA30 August 2010
2Allergovit Alnus/Corylus Stärke B, InjektionssuspensionA30 August 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
12 x 3 mlDurchstechflasche(n)V01AA07.13.3.A
21 x 3 mlDurchstechflasche(n)V01AA07.13.3.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Allergovit Alnus/Corylus Kombipackung authorised in Switzerland?

Yes. Allergovit Alnus/Corylus Kombipackung is authorised by Swissmedic under authorisation number 60624, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Allergovit Alnus/Corylus Kombipackung have?

Allergovit Alnus/Corylus 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 Alnus/Corylus 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.

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