Efexor ER 75 mg

Efexor ER 75 mg is a medicine authorised by Swissmedic under authorisation number 54168. The authorisation holder is Viatris Pharma GmbH. 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 25 June 1997 and the authorisation is valid without a time limit. ATC code N06AX16 places the medicine in the group Psychoanaleptics.

  • Dispensing category B
  • Authorisation number 54168
  • ATC N06AX16
  • Synthetic medicines
Authorisation data
Authorisation number54168
NameEfexor ER 75 mg
Full nameEfexor ER 75 mg, Hartkapsel, retardiert
Authorisation holderViatris Pharma GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN06AX16
First authorisation25 June 1997
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Efexor ER 75 mg, Hartkapsel, retardiertB25 June 1997
2Efexor ER 150 mg, Hartkapsel, retardiertB25 June 1997
4Efexor ER 37.5 mg, Hartkapsel, retardiertB09 February 2006

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1214Kapsel(n)N06AX1601.06.0.B
2028Kapsel(n)N06AX1601.06.0.B
3998Kapsel(n)N06AX1601.06.0.B
4714Kapsel(n)N06AX1601.06.0.B
5528Kapsel(n)N06AX1601.06.0.B
6398Kapsel(n)N06AX1601.06.0.B
717Kapsel(n)N06AX1601.06.0.B
7228Kapsel(n)N06AX1601.06.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Efexor ER 75 mg authorised in Switzerland?

Yes. Efexor ER 75 mg is authorised by Swissmedic under authorisation number 54168, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Efexor ER 75 mg have?

Efexor ER 75 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 Efexor ER 75 mg?

The authorisation holder is Viatris Pharma GmbH. 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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