Bonjesta 20 mg / 20 mg

Bonjesta 20 mg / 20 mg is a medicine authorised by Swissmedic under authorisation number 68867. The authorisation holder is Exeltis Suisse 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 05 December 2023 and the authorisation is limited until 04 December 2028. ATC code R06AA59 places the medicine in the group Antihistamines for systemic use.

  • Dispensing category B
  • Authorisation number 68867
  • ATC R06AA59
  • Synthetic medicines
Authorisation data
Authorisation number68867
NameBonjesta 20 mg / 20 mg
Full nameBonjesta 20 mg / 20 mg, Tablette mit veränderter Wirkstofffreisetzung
Authorisation holderExeltis Suisse SA
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeR06AA59
First authorisation05 December 2023
Authorisation validity04 December 2028
Strengths
No.NameDispensing categoryAuthorisation date
1Bonjesta 20 mg / 20 mg, Tablette mit veränderter WirkstofffreisetzungB05 December 2023

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Tablette(n)R06AA5901.09.0.B
220Tablette(n)R06AA5901.09.0.B
330Tablette(n)R06AA5901.09.0.B
440Tablette(n)R06AA5901.09.0.B
550Tablette(n)R06AA5901.09.0.B
660Tablette(n)R06AA5901.09.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Bonjesta 20 mg / 20 mg authorised in Switzerland?

Yes. Bonjesta 20 mg / 20 mg is authorised by Swissmedic under authorisation number 68867, data as of 01 September 2026. The authorisation is limited until 04 December 2028.

Which dispensing category does Bonjesta 20 mg / 20 mg have?

Bonjesta 20 mg / 20 mg 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 Bonjesta 20 mg / 20 mg?

The authorisation holder is Exeltis Suisse 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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