Rydapt 25 mg

Rydapt 25 mg is a medicine authorised by Swissmedic under authorisation number 66310. The authorisation holder is Novartis Pharma Schweiz AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 04 May 2017 and the authorisation is valid without a time limit. ATC code L01EX10 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 66310
  • ATC L01EX10
  • Synthetic medicines
Authorisation data
Authorisation number66310
NameRydapt 25 mg
Full nameRydapt 25 mg, Weichkapseln
Authorisation holderNovartis Pharma Schweiz AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01EX10
First authorisation04 May 2017
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Rydapt 25 mg, WeichkapselnA04 May 2017

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
156Kapsel(n)L01EX1007.16.1.A
2112Kapsel(n)L01EX1007.16.1.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Rydapt 25 mg authorised in Switzerland?

Yes. Rydapt 25 mg is authorised by Swissmedic under authorisation number 66310, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Rydapt 25 mg have?

Rydapt 25 mg is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.

Who is the authorisation holder of Rydapt 25 mg?

The authorisation holder is Novartis Pharma Schweiz 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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