Jivi 1000 IE

Jivi 1000 IE is a medicine authorised by Swissmedic under authorisation number 66882. The authorisation holder is Bayer (Schweiz) AG. The medicinal product code is Biotechnological medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 18 June 2019 and the authorisation is valid without a time limit. ATC code B02BD02 places the medicine in the group Antihemorrhagics.

  • Dispensing category B
  • Authorisation number 66882
  • ATC B02BD02
  • Biotechnological medicines
Authorisation data
Authorisation number66882
NameJivi 1000 IE
Full nameJivi 1000 IE, Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
Authorisation holderBayer (Schweiz) AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codeB02BD02
First authorisation18 June 2019
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
3Jivi 1000 IE, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungB18 June 2019
4Jivi 2000 IE, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungB18 June 2019
5Jivi 3000 IE, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungB18 June 2019

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
31SetB02BD0206.01.1.B
41SetB02BD0206.01.1.B
51SetB02BD0206.01.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Jivi 1000 IE authorised in Switzerland?

Yes. Jivi 1000 IE is authorised by Swissmedic under authorisation number 66882, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Jivi 1000 IE have?

Jivi 1000 IE is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.

Who is the authorisation holder of Jivi 1000 IE?

The authorisation holder is Bayer (Schweiz) 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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