Ibuprofen Viatris 200 mg

Ibuprofen Viatris 200 mg is a medicine authorised by Swissmedic under authorisation number 67940. The authorisation holder is Viatris Pharma GmbH. 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 12 June 2020 and the authorisation is valid without a time limit. ATC code M01AE01 places the medicine in the group Anti-inflammatory and antirheumatic products.

  • Dispensing category B
  • Authorisation number 67940
  • ATC M01AE01
  • Synthetic medicines
Authorisation data
Authorisation number67940
NameIbuprofen Viatris 200 mg
Full nameIbuprofen Viatris 200 mg, Filmtabletten
Authorisation holderViatris Pharma GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeM01AE01
First authorisation12 June 2020
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Ibuprofen Viatris 200 mg, FilmtablettenB12 June 2020
2Ibuprofen Viatris 400 mg, FilmtablettenB12 June 2020
3Ibuprofen Viatris 600 mg, FilmtablettenB12 June 2020

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
630Tablette(n)M01AE0107.10.1.B
720Tablette(n)M01AE0107.10.1.B
850Tablette(n)M01AE0107.10.1.B
920Tablette(n)M01AE0107.10.1.B
10100Tablette(n)M01AE0107.10.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ibuprofen Viatris 200 mg authorised in Switzerland?

Yes. Ibuprofen Viatris 200 mg is authorised by Swissmedic under authorisation number 67940, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Ibuprofen Viatris 200 mg have?

Ibuprofen Viatris 200 mg 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 Ibuprofen Viatris 200 mg?

The authorisation holder is Viatris Pharma GmbH. 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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