Ituxredi 100 mg/ 10 ml

Ituxredi 100 mg/ 10 ml is a medicine authorised by Swissmedic under authorisation number 70350. The authorisation holder is Dr. Reddy's Laboratories SA. The medicinal product code is Biotechnological 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 22 January 2026 and the authorisation is limited until 21 January 2031. ATC code L01FA01 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 70350
  • ATC L01FA01
  • Biotechnological medicines
Authorisation data
Authorisation number70350
NameItuxredi 100 mg/ 10 ml
Full nameItuxredi 100 mg/ 10 ml, Konzentrat zur Herstellung einer Infusionslösung
Authorisation holderDr. Reddy's Laboratories SA
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01FA01
First authorisation22 January 2026
Authorisation validity21 January 2031
Strengths
No.NameDispensing categoryAuthorisation date
1Ituxredi 100 mg/ 10 ml, Konzentrat zur Herstellung einer InfusionslösungA22 January 2026
2Ituxredi 500 mg/ 50 ml, Konzentrat zur Herstellung einer InfusionslösungA22 January 2026

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
12Durchstechflasche(n)L01FA0107.16.1.A
21Durchstechflasche(n)L01FA0107.16.1.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ituxredi 100 mg/ 10 ml authorised in Switzerland?

Yes. Ituxredi 100 mg/ 10 ml is authorised by Swissmedic under authorisation number 70350, data as of 01 September 2026. The authorisation is limited until 21 January 2031.

Which dispensing category does Ituxredi 100 mg/ 10 ml have?

Ituxredi 100 mg/ 10 ml 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 Ituxredi 100 mg/ 10 ml?

The authorisation holder is Dr. Reddy's Laboratories SA. 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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