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    Approved Drug Products containing 210954 listed in the FDA Orange Book. Original Data : FDA Website

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    Amneal Pharmaceuticals

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    01 AMNEAL PHARMS CO (3)

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    01 TABLET, DELAYED RELEASE;ORAL (3)

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    01 ERYTHROMYCIN (3)

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    ERYTHROMYCIN

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    TABLET, DELAYED RE...
    333MG
    2019-07-02
    210954
    ERYTHROMYCIN
    RX
    No
    AB
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    ERYTHROMYCIN

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    TABLET, DELAYED RE...
    500MG
    2019-07-02
    210954
    ERYTHROMYCIN
    RX
    No
    AB
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    ERYTHROMYCIN

    PDF Supplier PDF
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    TABLET, DELAYED RE...
    250MG
    2019-07-02
    210954
    ERYTHROMYCIN
    RX
    No
    AB
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    Looking for FDA Orange Book APPLICATION 210954

    Looking for FDA Orange Book APPLICATION 210954 3

    19

    Amneal Pharmaceuticals, 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 ERYTHROMYCIN, with a corresponding application number 210954.

    Regulatory Information RX

    With a dosage strength 333MG

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2019-07-02

    Therapeutic Equivalence (TE) Code AB

    18

    Amneal Pharmaceuticals, 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 ERYTHROMYCIN, with a corresponding application number 210954.

    Regulatory Information RX

    With a dosage strength 500MG

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2019-07-02

    Therapeutic Equivalence (TE) Code AB

    17

    Amneal Pharmaceuticals, 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 ERYTHROMYCIN, with a corresponding application number 210954.

    Regulatory Information RX

    With a dosage strength 250MG

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2019-07-02

    Therapeutic Equivalence (TE) Code AB

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