Pamorelin LA 11.25 mg

Pamorelin LA 11.25 mg is a medicine authorised by Swissmedic under authorisation number 56349. The authorisation holder is Debiopharm Research & Manufacturing SA. The medicinal product code is Synthetic 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 February 2005 and the authorisation is valid without a time limit. ATC code L02AE04 places the medicine in the group Endocrine therapy.

  • Dispensing category A
  • Authorisation number 56349
  • ATC L02AE04
  • Synthetic medicines
Authorisation data
Authorisation number56349
NamePamorelin LA 11.25 mg
Full namePamorelin LA 11.25 mg, poudre et solvant pour suspension injectable à libération prolongée
Authorisation holderDebiopharm Research & Manufacturing SA
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL02AE04
First authorisation09 February 2005
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Pamorelin LA 11.25 mg, poudre et solvant pour suspension injectable à libération prolongéeA09 February 2005
3Pamorelin LA 11.25 mg, poudre et solvant pour suspension injectable à libération prolongéeA07 September 2018

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
21SetL02AE0407.16.2.A
11SetL02AE0407.16.2.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Pamorelin LA 11.25 mg authorised in Switzerland?

Yes. Pamorelin LA 11.25 mg is authorised by Swissmedic under authorisation number 56349, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Pamorelin LA 11.25 mg have?

Pamorelin LA 11.25 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 Pamorelin LA 11.25 mg?

The authorisation holder is Debiopharm Research & Manufacturing 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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