Vydura 75 mg

Vydura 75 mg is a medicine authorised by Swissmedic under authorisation number 69035. The authorisation holder is Pfizer 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 18 October 2023 and the authorisation is limited until 17 October 2028. ATC code N02CD06 places the medicine in the group Analgesics.

  • Dispensing category B
  • Authorisation number 69035
  • ATC N02CD06
  • Synthetic medicines
Authorisation data
Authorisation number69035
NameVydura 75 mg
Full nameVydura 75 mg, Lyophilisat zum Einnehmen
Authorisation holderPfizer AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN02CD06
First authorisation18 October 2023
Authorisation validity17 October 2028
Strengths
No.NameDispensing categoryAuthorisation date
1Vydura 75 mg, Lyophilisat zum EinnehmenB18 October 2023

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
12Einzeldose(n)N02CD0602.05.1.B
28Einzeldose(n)N02CD0602.05.1.B
316Einzeldose(n)N02CD0602.05.1.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Vydura 75 mg authorised in Switzerland?

Yes. Vydura 75 mg is authorised by Swissmedic under authorisation number 69035, data as of 01 September 2026. The authorisation is limited until 17 October 2028.

Which dispensing category does Vydura 75 mg have?

Vydura 75 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 Vydura 75 mg?

The authorisation holder is Pfizer 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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