Suprelorin

Authorised

This medicine is authorised for use in the European Union

deslorelin acetate

Overview

Up-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information website

Suprelorin : EPAR - Summary for the public

Product information

Suprelorin : EPAR - Product Information

Suprelorin : EPAR - All Authorised presentations

Product details

• Name of medicine:
  Suprelorin
• Active substance:
  deslorelin acetate
• International non-proprietary name (INN) or common name:
  deslorelin acetate

Pharmacotherapeutic group

Pituitary and hypothalamic hormones and analogues

Authorisation details

• EMA product number:
  EMEA/V/C/000109

Assessment history

Changes since initial authorisation of medicine

Suprelorin : EPAR - Procedural steps taken and scientific information after authorisation

CVMP post-authorisation summary of positive opinion for Suprelorin (II-0032-G)

Adopted Reference Number: EMA/CVMP/250532/2022

Suprelorin-V-C-109-II-07 : EPAR - Assessment Report - Variation

Adopted Reference Number: EMA/520034/2012

CVMP post-authorisation summary of positive opinion for Suprelorin

Adopted Reference Number: EMA/CVMP/407323/2011

CVMP post-authorisation summary of positive opinion for Suprelorin

Adopted Reference Number: EMA/CVMP/149474/2010

Initial marketing authorisation documents

Suprelorin : EPAR - Procedural steps taken before authorisation

Suprelorin : EPAR - Scientific Discussion