Fintepla 2.2 mg/ml

Fintepla 2.2 mg/ml is a medicine authorised by Swissmedic under authorisation number 69371. The authorisation holder is UCB-Pharma SA. 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 13 February 2025 and the authorisation is limited until 12 February 2030. ATC code N03AX26 places the medicine in the group Antiepileptics.

  • Dispensing category A
  • Authorisation number 69371
  • ATC N03AX26
  • Synthetic medicines
Authorisation data
Authorisation number69371
NameFintepla 2.2 mg/ml
Full nameFintepla 2.2 mg/ml, solution buvable
Authorisation holderUCB-Pharma SA
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeN03AX26
First authorisation13 February 2025
Authorisation validity12 February 2030
Strengths
No.NameDispensing categoryAuthorisation date
1Fintepla 2.2 mg/ml, solution buvableA13 February 2025

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1120 mlFlasche(n)N03AX2601.07.1.A
2360 mlFlasche(n)N03AX2601.07.1.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Fintepla 2.2 mg/ml authorised in Switzerland?

Yes. Fintepla 2.2 mg/ml is authorised by Swissmedic under authorisation number 69371, data as of 01 September 2026. The authorisation is limited until 12 February 2030.

Which dispensing category does Fintepla 2.2 mg/ml have?

Fintepla 2.2 mg/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 Fintepla 2.2 mg/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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