Humatrope 6 mg

Humatrope 6 mg is a medicine authorised by Swissmedic under authorisation number 53052. The authorisation holder is Eli Lilly (Suisse) SA. 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 09 July 1996 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 53052
  • ATC H01AC01
  • Biotechnological medicines
Authorisation data
Authorisation number53052
NameHumatrope 6 mg
Full nameHumatrope 6 mg, poudre et solvant pour solution injectable
Authorisation holderEli Lilly (Suisse) SA
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeH01AC01
First authorisation09 July 1996
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Humatrope 6 mg, poudre et solvant pour solution injectableA09 July 1996
2Humatrope 12 mg, poudre et solvant pour solution injectableA09 July 1996
3Humatrope 24 mg, poudre et solvant pour solution injectableA09 July 1996

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
451 + 1Zylinderampulle(n)H01AC0107.03.1.A
531 + 1Zylinderampulle(n)H01AC0107.03.1.A
611 + 1Zylinderampulle(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 Humatrope 6 mg authorised in Switzerland?

Yes. Humatrope 6 mg is authorised by Swissmedic under authorisation number 53052, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Humatrope 6 mg have?

Humatrope 6 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 Humatrope 6 mg?

The authorisation holder is Eli Lilly (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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