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    Bromodiphenhydramine

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    REF. STANDARDS & IMPURITIES

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    01 1Actavis Inc

    02 1Forest Laboratories

    03 1Pfizer Inc

    04 1Wockhardt

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    01

    Actavis Inc

    Ireland
    Medlab Asia & Asia Health
    Not Confirmed
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    Actavis Inc

    Ireland
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    Medlab Asia & Asia Health
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    Regulatory Info : DISCN

    Registration Country : USA

    BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE

    Brand Name : BROMANYL

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 12.5MG/5ML;10MG/5ML

    Packaging :

    Approval Date : 1984-08-15

    Application Number : 88343

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Forest Laboratories

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Forest Laboratories

    U.S.A
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    Medlab Asia & Asia Health
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE

    Brand Name : AMBENYL

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 12.5MG/5ML;10MG/5ML

    Packaging :

    Approval Date : 1984-01-10

    Application Number : 9319

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Pfizer Inc

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Medlab Asia & Asia Health
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    Regulatory Info : DISCN

    Registration Country : USA

    BROMODIPHENHYDRAMINE HYDROCHLORIDE

    Brand Name : AMBODRYL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 7984

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Wockhardt

    India
    Medlab Asia & Asia Health
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    Wockhardt

    India
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    Medlab Asia & Asia Health
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    Regulatory Info : DISCN

    Registration Country : USA

    BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE

    Brand Name : BROMODIPHENHYDRAMINE HYDROCHLORIDE AND CODEINE PHOSPHATE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 12.5MG/5ML;10MG/5ML

    Packaging :

    Approval Date : 1984-10-12

    Application Number : 88626

    Regulatory Info : DISCN

    Registration Country : USA

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