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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Ropinirole Hydrochloride

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 3MG BASE

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    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Brand Name : REQUIP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 0.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-09-19

    Application Number : 20658

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    Brand Name : REQUIP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-09-19

    Application Number : 20658

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    Brand Name : REQUIP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-09-19

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    Brand Name : REQUIP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-09-19

    Application Number : 20658

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    Brand Name : REQUIP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-09-19

    Application Number : 20658

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    Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1999-01-27

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1999-01-27

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    Brand Name : REQUIP XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-06-13

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    Brand Name : REQUIP XL

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    Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-06-13

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    Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-06-13

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    Dosage Strength : EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-06-13

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    Brand Name : REQUIP XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-10-31

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    Dosage Strength : EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2009-04-10

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    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 0.25MG BASE

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    Approval Date : 2008-05-05

    Application Number : 77852

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    Dosage Strength : EQ 0.5MG BASE

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    Approval Date : 2008-05-05

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    Regulatory Info : DISCN

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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 77852

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Hikma Pharmaceuticals

    United Kingdom
    German Wound Congress
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    German Wound Congress
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    • fda
    • EDQM
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    Regulatory Info : DISCN

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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 77852

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Hikma Pharmaceuticals

    United Kingdom
    German Wound Congress
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 3MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 77852

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    Hikma Pharmaceuticals

    United Kingdom
    German Wound Congress
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 77852

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Hikma Pharmaceuticals

    United Kingdom
    German Wound Congress
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2008-05-19

    Application Number : 77852

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Prinston

    U.S.A
    German Wound Congress
    Not Confirmed
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    Prinston

    U.S.A
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 0.25MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 78110

    Regulatory Info : RX

    Registration Country : USA

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    29

    Prinston

    U.S.A
    German Wound Congress
    Not Confirmed
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    Prinston

    U.S.A
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

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    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 78110

    Regulatory Info : RX

    Registration Country : USA

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    30

    Prinston

    U.S.A
    German Wound Congress
    Not Confirmed
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    Prinston

    U.S.A
    arrow
    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : RX

    Registration Country : USA

    ROPINIROLE HYDROCHLORIDE

    Brand Name : ROPINIROLE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 2008-05-05

    Application Number : 78110

    Regulatory Info : RX

    Registration Country : USA

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