01 6Neuraxpharm
02 7Pluviaendo
03 57UCB Pharma S.A
01 6FILM, EXTENDED RELEASE;TRANSDERMAL
02 11Matrixpfl
03 6PATCH
04 6Patches
05 1Rotigotina 2Mg/Day 7 Plasters Transdermal Use
06 1Rotigotina 2Mg/Die 28 Plasters Transdermal Use
07 1Rotigotina 4Mg/Day 7 Plasters Transdermal Use
08 1Rotigotina 4Mg/Die 28 Plasters Transdermal Use
09 1Rotigotina 6Mg/Day 7 Plasters Transdermal Use
10 1Rotigotina 6Mg/Die 28 Plasters Transdermal Use
11 1Rotigotina 8Mg/Day 7 Plasters Transdermal Use
12 1Rotigotina 8Mg/Die 28 Plasters Transdermal Use
13 14TRANSDERMAL PATCH
14 7Transdermal Patch
15 8Transdermal patches
16 4Blank
01 6Prescription
02 6RX
03 58Blank
01 7Leganto
02 12NEUPRO
03 38Neupro
04 13Blank
01 4Australia
02 6Canada
03 8Italy
04 8Norway
05 6Spain
06 14Sweden
07 11Switzerland
08 7Turkey
09 6USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 2MG/24HR
Packaging :
Approval Date : 2007-05-09
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 4MG/24HR
Packaging :
Approval Date : 2007-05-09
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 6MG/24HR
Packaging :
Approval Date : 2007-05-09
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 1MG/24HR
Packaging :
Approval Date : 2012-04-02
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 3MG/24HR
Packaging :
Approval Date : 2012-04-02
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 8MG/24HR
Packaging :
Approval Date : 2012-04-02
Application Number : 21829
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 1 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 2 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 8 MG / 24 HOURS
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 6 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 3 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 4 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Leganto
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : POWER SERIES
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 1 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 3 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 6 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 4 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 8 MG / 24 HOURS
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : 2 MG / 24 H
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Neupro
Dosage Form : TRANSDERMAL PATCH
Dosage Strength : POWER SERIES
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 2Mg/Die 28 Plasters Transdermal Use
Dosage Strength : 28 transd plasters 2 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 2Mg/Day 7 Plasters Transdermal Use
Dosage Strength : 7 transd plasters 2 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 4Mg/Die 28 Plasters Transdermal Use
Dosage Strength : 28 transd plasters 4 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 4Mg/Day 7 Plasters Transdermal Use
Dosage Strength : 7 transd plasters 4 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 6Mg/Die 28 Plasters Transdermal Use
Dosage Strength : 28 transd plasters 6 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 6Mg/Day 7 Plasters Transdermal Use
Dosage Strength : 7 transd plasters 6 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 8Mg/Die 28 Plasters Transdermal Use
Dosage Strength : 28 transd plasters 8 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Neupro
Dosage Form : Rotigotina 8Mg/Day 7 Plasters Transdermal Use
Dosage Strength : 7 transd plasters 8 mg/day
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Neupro
Dosage Form : Transdermal patches
Dosage Strength : 2 mg/24 hours
Packaging : Dose Bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Neupro
Dosage Form : Transdermal patches
Dosage Strength : 2 mg/24 hours
Packaging : Dose Bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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