Paclitaxel-Teva 30 mg/5 ml

Paclitaxel-Teva 30 mg/5 ml is a medicine authorised by Swissmedic under authorisation number 57058. 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 16 August 2005 and the authorisation is valid without a time limit. The export lists no ATC code for this medicine.

  • Dispensing category A
  • Authorisation number 57058
  • Synthetic medicines
Authorisation data
Authorisation number57058
NamePaclitaxel-Teva 30 mg/5 ml
Full namePaclitaxel-Teva 30 mg/5 ml, Konzentrat zur Herstellung einer Infusionslösung
Authorisation holderTeva Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codenot stated
First authorisation16 August 2005
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Paclitaxel-Teva 30 mg/5 ml, Konzentrat zur Herstellung einer InfusionslösungA16 August 2005
2Paclitaxel-Teva 100 mg/16.7 ml, Konzentrat zur Herstellung einer InfusionslösungA16 August 2005
3Paclitaxel-Teva 300 mg/50 ml, Konzentrat zur Herstellung einer InfusionslösungA16 August 2005

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
The Swissmedic export lists no pack sizes for this medicine.

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Other medicines from this authorisation holder

Frequently asked questions

Is Paclitaxel-Teva 30 mg/5 ml authorised in Switzerland?

Yes. Paclitaxel-Teva 30 mg/5 ml is authorised by Swissmedic under authorisation number 57058, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Paclitaxel-Teva 30 mg/5 ml have?

Paclitaxel-Teva 30 mg/5 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 Paclitaxel-Teva 30 mg/5 ml?

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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