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    Approved Drug Products containing 19712 listed in the FDA Orange Book. Original Data : FDA Website

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    01 AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER (1)

    02 AMINOSYN II 4.25% W/ ELECT AND ADJUSTED PHOSPHATE IN DEXTROSE 10% IN PLASTIC CONTAINER (1)

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    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

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    INJECTABLE; INJECT...
    4.25%;10GM/100ML;5...
    1988-09-08
    19712
    AMINOSYN II 4.25% ...
    DISCN
    No
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    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    PDF Supplier PDF
    URL Supplier Web Content
    INJECTABLE; INJECT...
    3.5%;5GM/100ML;30M...
    1988-09-08
    19712
    AMINOSYN II 3.5% M...
    DISCN
    No
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    Looking for FDA Orange Book APPLICATION 19712

    Looking for FDA Orange Book APPLICATION 19712 2

    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 AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE, with a corresponding application number 19712.

    Regulatory Information DISCN

    With a dosage strength 4.25%;10GM/100ML;51MG/100ML;176.5MG/100ML;22.4MG/100ML;104.5MG/100ML;205MG/100ML

    Dosage Form Route INJECTABLE; INJECTION

    Reference Listed Drug No

    Approved since 1988-09-08

    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 AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, with a corresponding application number 19712.

    Regulatory Information DISCN

    With a dosage strength 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Dosage Form Route INJECTABLE; INJECTION

    Reference Listed Drug No

    Approved since 1988-09-08

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