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    Romifidine

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1Boehringer Ingelheim Vetmedica GmbH

    02 1Boehringer Ingelheim Vetmedica Gmbh

    03 1Le Vet Beheer BV

    04 1Le Vet Beheer Bv

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    Boehringer Ingelheim Vetmedica GmbH

    Germany
    BioProcess International US West
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    Boehringer Ingelheim Vetmedica GmbH

    Germany
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    BioProcess International US West
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    Regulatory Info : Marketed

    Registration Country : Norway

    Romifidinhydroklorid

    Brand Name : Sedivet vet

    Dosage Form : Solution For Injection

    Dosage Strength : 10mg/ml

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Marketed

    Registration Country : Norway

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    02

    Boehringer Ingelheim Vetmedica Gmbh

    Germany
    BioProcess International US West
    Not Confirmed
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    Boehringer Ingelheim Vetmedica Gmbh

    Germany
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    BioProcess International US West
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Romifidin Hydrochloride

    Brand Name : Sedivet Vet.

    Dosage Form : Injection Solution

    Dosage Strength : 10mg/ml

    Packaging :

    Approval Date : 26-07-1995

    Application Number : 28101489692

    Regulatory Info : Prescription

    Registration Country : Denmark

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    03

    Le Vet Beheer BV

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    BioProcess International US West
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    Le Vet Beheer BV

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    Regulatory Info : Marketed

    Registration Country : Norway

    Romifidinhydroklorid

    Brand Name : Rominervin vet

    Dosage Form : Solution For Injection

    Dosage Strength : 10mg/ml

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    Approval Date :

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    Regulatory Info : Marketed

    Registration Country : Norway

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    04

    Le Vet Beheer Bv

    Country
    BioProcess International US West
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    Le Vet Beheer Bv

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Romifidin Hydrochloride

    Brand Name : Rominervin Vet.

    Dosage Form : Injection Solution

    Dosage Strength : 10mg/ml

    Packaging :

    Approval Date : 10-09-2018

    Application Number : 28106000817

    Regulatory Info : Prescription

    Registration Country : Denmark

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