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    Approved Drug Products containing 19005 listed in the FDA Orange Book. Original Data : FDA Website

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    01 BRETYLIUM TOSYLATE IN DEXTROSE 5% (3)

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    BRETYLIUM TOSYLATE

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    INJECTABLE; INJECT...
    200MG/100ML
    1986-04-29
    19005
    BRETYLIUM TOSYLATE...
    DISCN
    No
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    BRETYLIUM TOSYLATE

    PDF Supplier PDF
    URL Supplier Web Content
    INJECTABLE; INJECT...
    400MG/100ML
    1986-04-29
    19005
    BRETYLIUM TOSYLATE...
    DISCN
    No
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    your Marketing & Sales content
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    • EDQM
    • WHO-GMP
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    BRETYLIUM TOSYLATE

    PDF Supplier PDF
    URL Supplier Web Content
    INJECTABLE; INJECT...
    800MG/100ML
    1986-04-29
    19005
    BRETYLIUM TOSYLATE...
    DISCN
    No
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    Looking for FDA Orange Book APPLICATION 19005

    Looking for FDA Orange Book APPLICATION 19005 3

    19

    Abbott Laboratories, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is BRETYLIUM TOSYLATE, with a corresponding application number 19005.

    Regulatory Information DISCN

    With a dosage strength 200MG/100ML

    Dosage Form Route INJECTABLE; INJECTION

    Reference Listed Drug No

    Approved since 1986-04-29

    18

    Abbott Laboratories, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is BRETYLIUM TOSYLATE, with a corresponding application number 19005.

    Regulatory Information DISCN

    With a dosage strength 400MG/100ML

    Dosage Form Route INJECTABLE; INJECTION

    Reference Listed Drug No

    Approved since 1986-04-29

    17

    Abbott Laboratories, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is BRETYLIUM TOSYLATE, with a corresponding application number 19005.

    Regulatory Information DISCN

    With a dosage strength 800MG/100ML

    Dosage Form Route INJECTABLE; INJECTION

    Reference Listed Drug No

    Approved since 1986-04-29

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