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    Approved Drug Products containing 91426 listed in the FDA Orange Book. Original Data : FDA Website

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    Amneal Pharmaceuticals

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    01 AMNEAL PHARMS (3)

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    01 TABLET;ORAL (3)

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    01 RX (3)

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    01 SPIRONOLACTONE (3)

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    01 No (3)

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    SPIRONOLACTONE

    PDF Supplier PDF
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    TABLET; ORAL
    100MG
    2010-07-02
    91426
    SPIRONOLACTONE
    RX
    No
    AB
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    SPIRONOLACTONE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    25MG
    2010-07-02
    91426
    SPIRONOLACTONE
    RX
    No
    AB
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    • EDQM
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    SPIRONOLACTONE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    50MG
    2010-07-02
    91426
    SPIRONOLACTONE
    RX
    No
    AB
    ASK
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    PHARMACOMPASS
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    Looking for FDA Orange Book APPLICATION 91426

    Looking for FDA Orange Book APPLICATION 91426 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 SPIRONOLACTONE, with a corresponding application number 91426.

    Regulatory Information RX

    With a dosage strength 100MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2010-07-02

    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 SPIRONOLACTONE, with a corresponding application number 91426.

    Regulatory Information RX

    With a dosage strength 25MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2010-07-02

    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 SPIRONOLACTONE, with a corresponding application number 91426.

    Regulatory Information RX

    With a dosage strength 50MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2010-07-02

    Therapeutic Equivalence (TE) Code AB

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