Xeplion 25 mg

Xeplion 25 mg is a medicine authorised by Swissmedic under authorisation number 60466. The authorisation holder is Janssen-Cilag AG. 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 15 December 2010 and the authorisation is valid without a time limit. ATC code N05AX13 places the medicine in the group Psycholeptics.

  • Dispensing category B
  • Authorisation number 60466
  • ATC N05AX13
  • Synthetic medicines
Authorisation data
Authorisation number60466
NameXeplion 25 mg
Full nameXeplion 25 mg, Depot-Injektionssuspension in einer Fertigspritze
Authorisation holderJanssen-Cilag AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN05AX13
First authorisation15 December 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Xeplion 25 mg, Depot-Injektionssuspension in einer FertigspritzeB15 December 2010
2Xeplion 50 mg, Depot-Injektionssuspension in einer FertigspritzeB15 December 2010
3Xeplion 75 mg, Depot-Injektionssuspension in einer FertigspritzeB15 December 2010
4Xeplion 100 mg, Depot-Injektionssuspension in einer FertigspritzeB15 December 2010
5Xeplion 150 mg, Depot-Injektionssuspension in einer FertigspritzeB15 December 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Fertigspritze(n)N05AX1301.05.0.B
21Fertigspritze(n)N05AX1301.05.0.B
31Fertigspritze(n)N05AX1301.05.0.B
41Fertigspritze(n)N05AX1301.05.0.B
51Fertigspritze(n)N05AX1301.05.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Xeplion 25 mg authorised in Switzerland?

Yes. Xeplion 25 mg is authorised by Swissmedic under authorisation number 60466, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Xeplion 25 mg have?

Xeplion 25 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 Xeplion 25 mg?

The authorisation holder is Janssen-Cilag 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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