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List of All Manufacturers & Suppliers of rotigotine transdermal patch Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 13,273Xls
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01 6Neuraxpharm

02 7Pluviaendo

03 57UCB Pharma S.A

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01

34th IFSCC
Not Confirmed
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34th IFSCC
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ROTIGOTINE

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

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02

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

ROTIGOTINE

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

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03

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

ROTIGOTINE

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

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04

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

ROTIGOTINE

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

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05

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

ROTIGOTINE

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

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06

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

ROTIGOTINE

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

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07

34th IFSCC
Not Confirmed
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34th IFSCC
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rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 1 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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08

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 2 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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09

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 8 MG / 24 HOURS

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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10

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 6 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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11

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 3 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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12

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 4 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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13

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Leganto

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : POWER SERIES

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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14

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 1 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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15

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 3 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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16

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 6 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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17

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 4 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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18

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 8 MG / 24 HOURS

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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19

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : 2 MG / 24 H

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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20

34th IFSCC
Not Confirmed
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34th IFSCC
Not Confirmed

rotigotine

Brand Name : Neupro

Dosage Form : TRANSDERMAL PATCH

Dosage Strength : POWER SERIES

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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