Genotropin 12 mg

Genotropin 12 mg is a medicine authorised by Swissmedic under authorisation number 50823. The authorisation holder is Pfizer AG. The medicinal product code is Biotechnological 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 23 May 1990 and the authorisation is valid without a time limit. ATC code H01AC01 places the medicine in the group Pituitary and hypothalamic hormones and analogues.

  • Dispensing category A
  • Authorisation number 50823
  • ATC H01AC01
  • Biotechnological medicines
Authorisation data
Authorisation number50823
NameGenotropin 12 mg
Full nameGenotropin 12 mg, Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
Authorisation holderPfizer AG
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeH01AC01
First authorisation23 May 1990
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
2Genotropin 12 mg, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungA03 April 1996
3Genotropin 5 mg, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungA28 September 2000

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1051 x 12 mgAmpulle(n)H01AC0107.03.1.A
1135 x 5 mgAmpulle(n)H01AC0107.03.1.A
1211 x 5 mgAmpulle(n)H01AC0107.03.1.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Genotropin 12 mg authorised in Switzerland?

Yes. Genotropin 12 mg is authorised by Swissmedic under authorisation number 50823, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Genotropin 12 mg have?

Genotropin 12 mg 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 Genotropin 12 mg?

The authorisation holder is Pfizer 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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