Neupro 3 mg/24 h transdermal patch

Active Ingredient
Strength
  • Rotigotine: 3 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/1/05/331/47 3 mg N04BC Transdermal patch
EU/1/05/331/48 3 mg N04BC Transdermal patch
EU/1/05/331/49 3 mg N04BC Transdermal patch
EU/1/05/331/50 3 mg N04BC Transdermal patch
EU/1/05/331/51 3 mg N04BC Transdermal patch
EU/1/05/331/52 3 mg N04BC Transdermal patch
EU/1/05/331/53 3 mg N04BC Transdermal patch
EU/1/05/331/54 3 mg N04BC Transdermal patch
EU/1/05/331/55 3 mg N04BC Transdermal patch
Licence number
EU/1/05/331/47
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/48
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/49
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/50
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/51
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/52
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/53
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/54
Strength
3 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/55
Strength
3 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