Axotide Diskus 100

Axotide Diskus 100 is a medicine authorised by Swissmedic under authorisation number 53390. The authorisation holder is GlaxoSmithKline 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 29 August 1995 and the authorisation is valid without a time limit. ATC code R03BA05 places the medicine in the group Drugs for obstructive airway diseases.

  • Dispensing category B
  • Authorisation number 53390
  • ATC R03BA05
  • Synthetic medicines
Authorisation data
Authorisation number53390
NameAxotide Diskus 100
Full nameAxotide Diskus 100, Mutlidosen-Pulverinhalator
Authorisation holderGlaxoSmithKline AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeR03BA05
First authorisation29 August 1995
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Axotide Diskus 100, Mutlidosen-PulverinhalatorB29 August 1995
2Axotide Diskus 250, Mutlidosen-PulverinhalatorB29 August 1995
3Axotide Diskus 500, Mutlidosen-PulverinhalatorB29 August 1995

Scroll the table sideways

Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1360InhalationenR03BA0503.04.4.B
2160InhalationenR03BA0503.04.4.B
4860InhalationenR03BA0503.04.4.B

Scroll the table sideways

Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Axotide Diskus 100 authorised in Switzerland?

Yes. Axotide Diskus 100 is authorised by Swissmedic under authorisation number 53390, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Axotide Diskus 100 have?

Axotide Diskus 100 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 Axotide Diskus 100?

The authorisation holder is GlaxoSmithKline 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.

Authorisation in Switzerland?

About 2 minutes. No obligation.

First, a little about your business.

Your answers stay in this page until you send your enquiry.

What would you like to achieve?

Your project

Where can we reach you?

You can go back to review your answers before sending.

* Required fields
Prefer email? info@swissmedicinesdirectory.com