Colistin zur Infusion 1 Mio IE

Colistin zur Infusion 1 Mio IE is a medicine authorised by Swissmedic under authorisation number 67406. 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 12 May 2020 and the authorisation is valid without a time limit. ATC code J01XB01 places the medicine in the group Antibacterials for systemic use.

  • Dispensing category A
  • Authorisation number 67406
  • ATC J01XB01
  • Synthetic medicines
Authorisation data
Authorisation number67406
NameColistin zur Infusion 1 Mio IE
Full nameColistin zur Infusion 1 Mio IE, Pulver zur Herstellung einer Infusionslösung
Authorisation holderTeva Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeJ01XB01
First authorisation12 May 2020
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Colistin zur Infusion 1 Mio IE, Pulver zur Herstellung einer InfusionslösungA12 May 2020
2Colistin zur Infusion 2 Mio IE, Pulver zur Herstellung einer InfusionslösungA12 May 2020

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Durchstechflasche(n)J01XB0108.01.9.A
210Durchstechflasche(n)J01XB0108.01.9.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Colistin zur Infusion 1 Mio IE authorised in Switzerland?

Yes. Colistin zur Infusion 1 Mio IE is authorised by Swissmedic under authorisation number 67406, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Colistin zur Infusion 1 Mio IE have?

Colistin zur Infusion 1 Mio IE 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 Colistin zur Infusion 1 Mio IE?

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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