Briviact 50 mg/5 ml

Briviact 50 mg/5 ml is a medicine authorised by Swissmedic under authorisation number 65830. The authorisation holder is UCB-Pharma SA. The medicinal product code is Synthetic 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 06 October 2016 and the authorisation is valid without a time limit. ATC code N03AX23 places the medicine in the group Antiepileptics.

  • Dispensing category B
  • Authorisation number 65830
  • ATC N03AX23
  • Synthetic medicines
Authorisation data
Authorisation number65830
NameBriviact 50 mg/5 ml
Full nameBriviact 50 mg/5 ml, solution injectable
Authorisation holderUCB-Pharma SA
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN03AX23
First authorisation06 October 2016
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Briviact 50 mg/5 ml, solution injectableB06 October 2016

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Durchstechflasche(n)N03AX2301.07.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Briviact 50 mg/5 ml authorised in Switzerland?

Yes. Briviact 50 mg/5 ml is authorised by Swissmedic under authorisation number 65830, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Briviact 50 mg/5 ml have?

Briviact 50 mg/5 ml 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 Briviact 50 mg/5 ml?

The authorisation holder is UCB-Pharma SA. 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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