Neupro 1 mg/24 h transdermal patch

Active Ingredient
Strength
  • Rotigotine: 1 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/1/05/331/38 1 mg N04BC Transdermal patch
EU/1/05/331/39 1 mg N04BC Transdermal patch
EU/1/05/331/40 1 mg N04BC Transdermal patch
EU/1/05/331/41 1 mg N04BC Transdermal patch
EU/1/05/331/42 1 mg N04BC Transdermal patch
EU/1/05/331/43 1 mg N04BC Transdermal patch
EU/1/05/331/44 1 mg N04BC Transdermal patch
EU/1/05/331/45 1 mg N04BC Transdermal patch
EU/1/05/331/46 1 mg N04BC Transdermal patch
Licence number
EU/1/05/331/38
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/39
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/40
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/41
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/42
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/43
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/44
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/45
Strength
1 mg
ATC Code
N04BC
Dosage Form
Transdermal patch
Licence number
EU/1/05/331/46
Strength
1 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