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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.https://marketing.lgmpharma.com/LGM-CDMO

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    Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

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    Zuclopenthixol Acetate

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    2Care4 Aps

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Zuclopenthixol Acetate

    Brand Name : Clopixol-Acuphase

    Dosage Form : Injection Solution

    Dosage Strength : 50mg/ml

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    Approval Date : 28-09-2017

    Application Number : 28105992117

    Regulatory Info : Prescription

    Registration Country : Denmark

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    Ebb Medical Ab

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    Regulatory Info : Approved

    Registration Country : Sweden

    Zuclopenthixol Acetate

    Brand Name : Clopixol-Acutard

    Dosage Form : Injectable Solution

    Dosage Strength : 50mg/ml

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    Approval Date : 31-01-2018

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    Ebb Medical Ab

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    Regulatory Info : Approved

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    Zuclopenthixol Acetate

    Brand Name : Clopixol-Acutard

    Dosage Form : Injectable Solution

    Dosage Strength : 50mg/ml

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    Approval Date : 13-06-2024

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    LUNDBECK ITALIA SpA

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    Registration Country : Italy

    Zuclopenthixol Acetate

    Brand Name : Clopixol Acuphase

    Dosage Form :

    Dosage Strength : 1 Ampoule Im 50 Mg 1 Ml  

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    Registration Country : Italy

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    Lundbeck (Switzerland) Ag

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Zuclopenthixol Acetate

    Brand Name : Clopixol Acutard

    Dosage Form : Solution For Injection

    Dosage Strength : 50mg/ml

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    Approval Date : 02/12/1986

    Application Number : 47783

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    Lundbeck Limited

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    Regulatory Info : Withdrawn

    Registration Country : Malta

    Zuclopenthixol Acetate

    Brand Name : Clopixol-Acuphase

    Dosage Form : Solution For Injection

    Dosage Strength : 50MG/ML

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    Approval Date : 2006-02-14

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    Regulatory Info : Withdrawn

    Registration Country : Malta

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    H. Lundbeck A/S

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    Regulatory Info : Marketed

    Registration Country : Norway

    Zuklopentiksolacetat

    Brand Name : Cisordinol-Acutard

    Dosage Form : Solution For Injection

    Dosage Strength : 50mg/ml

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    Regulatory Info : Marketed

    Registration Country : Norway

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    Lundbeck Spain Sa

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    Regulatory Info : Authorized

    Registration Country : Spain

    Zuclopentixol Acetate

    Brand Name : Clopixol Acufase

    Dosage Form : Injectable Solution

    Dosage Strength : 50MG

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    Approval Date : 01-12-1995

    Application Number : 60875

    Regulatory Info : Authorized

    Registration Country : Spain

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    09

    H. Lundbeck A/S

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Zuclopenthixol Acetate

    Brand Name : Cisordinol-Acutard

    Dosage Form : Injection Solution

    Dosage Strength : 50mg/ml

    Packaging :

    Approval Date : 03-06-1986

    Application Number : 28101227785

    Regulatory Info : Prescription

    Registration Country : Denmark

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    10

    H. Lundbeck A/S

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    Regulatory Info : Approved

    Registration Country : Sweden

    Zuclopenthixol Acetate

    Brand Name : Cisordinol-Acutard

    Dosage Form : Injectable Solution

    Dosage Strength : 50mg/ml

    Packaging :

    Approval Date : 18-09-1987

    Application Number : 1.99E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.