Solu-Medrol 500 mg

Solu-Medrol 500 mg is a medicine authorised by Swissmedic under authorisation number 35112. 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 06 October 1969 and the authorisation is valid without a time limit. ATC code H02AB04 places the medicine in the group Corticosteroids for systemic use.

  • Dispensing category B
  • Authorisation number 35112
  • ATC H02AB04
  • Synthetic medicines
Authorisation data
Authorisation number35112
NameSolu-Medrol 500 mg
Full nameSolu-Medrol 500 mg, Pulver und Lösungsmittel zur Herstellung einer Injektions-/Infusionslösung
Authorisation holderPfizer AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeH02AB04
First authorisation06 October 1969
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
4Solu-Medrol 500 mg, Pulver und Lösungsmittel zur Herstellung einer Injektions-/InfusionslösungB16 December 1974
5Solu-Medrol 1 g, Pulver und Lösungsmittel zur Herstellung einer Injektions-/InfusionslösungB26 February 1976

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
811 + 1Durchstechflasche(n)H02AB0407.07.23B
571 + 1Durchstechflasche(n)H02AB0407.07.23B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Solu-Medrol 500 mg authorised in Switzerland?

Yes. Solu-Medrol 500 mg is authorised by Swissmedic under authorisation number 35112, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Solu-Medrol 500 mg have?

Solu-Medrol 500 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 Solu-Medrol 500 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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