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    Approved Drug Products containing 74910 listed in the FDA Orange Book. Original Data : FDA Website

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    01 MYLAN (3)

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    01 CAPSULE, EXTENDED RELEASE;ORAL (3)

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    01 RX (3)

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    01 DILTIAZEM HYDROCHLORIDE (3)

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    DILTIAZEM HYDROCHLORIDE

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    CAPSULE, EXTENDED ...
    90MG
    1997-05-02
    74910
    DILTIAZEM HYDROCHL...
    RX
    No
    AB1
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    DILTIAZEM HYDROCHLORIDE

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    CAPSULE, EXTENDED ...
    120MG
    1997-05-02
    74910
    DILTIAZEM HYDROCHL...
    RX
    No
    AB1
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    • EDQM
    • WHO-GMP
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    DILTIAZEM HYDROCHLORIDE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE, EXTENDED ...
    60MG
    1997-05-02
    74910
    DILTIAZEM HYDROCHL...
    RX
    No
    AB1
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    Looking for FDA Orange Book APPLICATION 74910

    Looking for FDA Orange Book APPLICATION 74910 3

    19

    Viatris, 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 DILTIAZEM HYDROCHLORIDE, with a corresponding application number 74910.

    Regulatory Information RX

    With a dosage strength 90MG

    Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 1997-05-02

    Therapeutic Equivalence (TE) Code AB1

    18

    Viatris, 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 DILTIAZEM HYDROCHLORIDE, with a corresponding application number 74910.

    Regulatory Information RX

    With a dosage strength 120MG

    Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 1997-05-02

    Therapeutic Equivalence (TE) Code AB1

    17

    Viatris, 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 DILTIAZEM HYDROCHLORIDE, with a corresponding application number 74910.

    Regulatory Information RX

    With a dosage strength 60MG

    Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 1997-05-02

    Therapeutic Equivalence (TE) Code AB1

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