Neupro 6 mg/24 h transdermal patch

Active Ingredient
Strength
  • Rotigotine: 6 mg
Dosage Form
Transdermal patch
Legal Category
A - prescription, may not be renewed
Last Updated
25/09/2026
Licence Info section shown.
Licence numbers with strength, ATC code and dosage form
Licence number Strength ATC Code Dosage Form
EU/1/05/331/7 6 mg N04BC Transdermal patch
EU/1/05/331/8 6 mg N04BC Transdermal patch
EU/1/05/331/9 6 mg N04BC Transdermal patch
EU/1/05/331/26 6 mg N04BC Transdermal patch
EU/1/05/331/27 6 mg N04BC Transdermal patch
EU/1/05/331/28 6 mg N04BC Transdermal patch
EU/1/05/331/29 6 mg N04BC Transdermal patch
EU/1/05/331/30 6 mg N04BC Transdermal patch
EU/1/05/331/31 6 mg N04BC Transdermal patch
Licence number
EU/1/05/331/7
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/8
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/9
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/26
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/27
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/28
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/29
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/30
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/31
Strength
6 mg
ATC Code
N04BC
Dosage Form
Transdermal patch

UCB (Pharma) Ireland Limited

United Drug House, Magna Drive, Magna Business Park, Citywest Road, Dublin 24, Ireland

Telephone
+3531800930075