Filgrastim-Teva 30 / 0.5 ml

Filgrastim-Teva 30 / 0.5 ml is a medicine authorised by Swissmedic under authorisation number 60722. The authorisation holder is Teva Pharma AG. 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 08 January 2010 and the authorisation is valid without a time limit. ATC code L03AA02 places the medicine in the group Immunostimulants.

  • Dispensing category A
  • Authorisation number 60722
  • ATC L03AA02
  • Biotechnological medicines
Authorisation data
Authorisation number60722
NameFilgrastim-Teva 30 / 0.5 ml
Full nameFilgrastim-Teva 30 / 0.5 ml, Injektionslösung in Fertigspritzen
Authorisation holderTeva Pharma AG
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL03AA02
First authorisation08 January 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Filgrastim-Teva 30 / 0.5 ml, Injektionslösung in FertigspritzenA08 January 2010
2Filgrastim-Teva 48 / 0.8 ml, Injektionslösung in FertigspritzenA08 January 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Spritze(n)L03AA0206.07.3.A
25Spritze(n)L03AA0206.07.3.A
41Spritze(n)L03AA0206.07.3.A
55Spritze(n)L03AA0206.07.3.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Filgrastim-Teva 30 / 0.5 ml authorised in Switzerland?

Yes. Filgrastim-Teva 30 / 0.5 ml is authorised by Swissmedic under authorisation number 60722, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Filgrastim-Teva 30 / 0.5 ml have?

Filgrastim-Teva 30 / 0.5 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 Filgrastim-Teva 30 / 0.5 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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