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01 6Exeltis
02 6Luye Pharma
03 6Medical Valley
04 7Pluviaendo
05 1Schwarz Pharma Limited
06 66UCB Pharma S.A
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01 6FILM, EXTENDED RELEASE;TRANSDERMAL
02 6PATCH
03 1Rotigotina 2Mg/Day 7 Plasters Transdermal Use
04 1Rotigotina 2Mg/Die 28 Plasters Transdermal Use
05 1Rotigotina 4Mg/Day 7 Plasters Transdermal Use
06 1Rotigotina 4Mg/Die 28 Plasters Transdermal Use
07 1Rotigotina 6Mg/Day 7 Plasters Transdermal Use
08 1Rotigotina 6Mg/Die 28 Plasters Transdermal Use
09 1Rotigotina 8Mg/Day 7 Plasters Transdermal Use
10 1Rotigotina 8Mg/Die 28 Plasters Transdermal Use
11 56Transdermal Patch
12 8Transdermal patches
13 8Blank
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01 6Allowed
02 13Approved
03 23Authorized
04 7Deregistered
05 6Prescription
06 6RX
07 31Blank
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01 6Dariant
02 7Leganto
03 12NEUPRO
04 42Neupro
05 6Neupro h
06 6Rotigotina Luye
07 6Rotigotine Medical Valley
08 7Blank
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01 8Australia
02 6Canada
03 8Italy
04 8Norway
05 23Spain
06 20Sweden
07 6Switzerland
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 : 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
Regulatory Info :
Registration Country : Norway
Brand Name : Neupro
Dosage Form : Transdermal patches
Dosage Strength : 4 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 : 4 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 : 6 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 : 6 mg/24 hours
Packaging : Dose Bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway