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    Dinoprost Tromethamine

    ACTIVE PHARMA INGREDIENTS

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    01 1CEVA ANIMAL HEALTH INC

    02 1Dong Bang Co., Ltd

    03 1Labiana Life Sciences S.A

    04 1Pfizer Inc

    05 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania

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    01

    CEVA ANIMAL HEALTH INC

    Canada
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    CEVA ANIMAL HEALTH INC

    Canada
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    Regulatory Info : Prescription

    Registration Country : Canada

    DINOPROST (DINOPROST TROMETHAMINE)

    Brand Name : ENZAPROST T

    Dosage Form : SOLUTION

    Dosage Strength : 5MG/ML

    Packaging : 10/10/30/50ML

    Approval Date :

    Application Number : 2468697

    Regulatory Info : Prescription

    Registration Country : Canada

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    02

    Dong Bang Co., Ltd

    South Korea
    Antibody Engineering
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    South Korea
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    Regulatory Info :

    Registration Country : South Korea

    Dinoprost Tromethamine

    Brand Name : Prolin

    Dosage Form : Injectable

    Dosage Strength : 5MG/ML

    Packaging : 10ML, 30ML Vials

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : South Korea

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    03

    Labiana Life Sciences S.A

    Spain
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    Regulatory Info :

    Registration Country :

    Dinoprost Tromethamine

    Brand Name : Prosyl®

    Dosage Form :

    Dosage Strength :

    Packaging : 5, 10, 20, 50 ML Vial

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country :

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    04

    Pfizer Inc

    U.S.A
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DINOPROST TROMETHAMINE

    Brand Name : PROSTIN F2 ALPHA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17434

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    ZOETIS MANUFACTURING ITALIA S.R.L. ...

    Italy
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    ZOETIS MANUFACTURING ITALIA S.R.L. ...

    Italy
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    Regulatory Info : Prescription

    Registration Country : Canada

    DINOPROST (DINOPROST TROMETHAMINE)

    Brand Name : LUTALYSE

    Dosage Form : SOLUTION

    Dosage Strength : 5MG/ML

    Packaging : 30ML/100ML

    Approval Date :

    Application Number : 813605

    Regulatory Info : Prescription

    Registration Country : Canada

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