Lenalidomid-Teva 2.5 mg

Lenalidomid-Teva 2.5 mg is a medicine authorised by Swissmedic under authorisation number 67460. The authorisation holder is Teva Pharma 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 05 November 2019 and the authorisation is valid without a time limit. ATC code L04AX04 places the medicine in the group Immunosuppressants.

  • Dispensing category A
  • Authorisation number 67460
  • ATC L04AX04
  • Synthetic medicines
Authorisation data
Authorisation number67460
NameLenalidomid-Teva 2.5 mg
Full nameLenalidomid-Teva 2.5 mg, Hartkapseln
Authorisation holderTeva Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL04AX04
First authorisation05 November 2019
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Lenalidomid-Teva 2.5 mg, HartkapselnA05 November 2019
2Lenalidomid-Teva 5 mg, HartkapselnA05 November 2019
3Lenalidomid-Teva 7.5 mg, HartkapselnA05 November 2019
4Lenalidomid-Teva 10 mg, HartkapselnA05 November 2019
5Lenalidomid-Teva 15 mg, HartkapselnA05 November 2019
6Lenalidomid-Teva 20 mg, HartkapselnA05 November 2019
7Lenalidomid-Teva 25 mg, HartkapselnA05 November 2019

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
121Kapsel(n)L04AX0407.16.4.A
221Kapsel(n)L04AX0407.16.4.A
321Kapsel(n)L04AX0407.16.4.A
421Kapsel(n)L04AX0407.16.4.A
521Kapsel(n)L04AX0407.16.4.A
621Kapsel(n)L04AX0407.16.4.A
721Kapsel(n)L04AX0407.16.4.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Lenalidomid-Teva 2.5 mg authorised in Switzerland?

Yes. Lenalidomid-Teva 2.5 mg is authorised by Swissmedic under authorisation number 67460, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Lenalidomid-Teva 2.5 mg have?

Lenalidomid-Teva 2.5 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 Lenalidomid-Teva 2.5 mg?

The authorisation holder is Teva Pharma 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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