Biodoron 150 mg

Biodoron 150 mg is a medicine authorised by Swissmedic under authorisation number 38051. The authorisation holder is Weleda AG. The medicinal product code is Anthroposophic 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 23 November 1982 and the authorisation is valid without a time limit. ATC code N02CX places the medicine in the group Analgesics.

  • Dispensing category B
  • Authorisation number 38051
  • ATC N02CX
  • Anthroposophic medicines
Authorisation data
Authorisation number38051
NameBiodoron 150 mg
Full nameBiodoron 150 mg, Hartkapseln
Authorisation holderWeleda AG
Medicinal product codeAnthroposophic medicines
Dispensing categoryB · Prescription only
ATC codeN02CX
First authorisation23 November 1982
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Biodoron 150 mg, HartkapselnB23 November 1982

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1620Kapsel(n)N02CX20.02.B
2480Kapsel(n)N02CX20.02.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Biodoron 150 mg authorised in Switzerland?

Yes. Biodoron 150 mg is authorised by Swissmedic under authorisation number 38051, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Biodoron 150 mg have?

Biodoron 150 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 Biodoron 150 mg?

The authorisation holder is Weleda 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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