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    Approved Drug Products containing 203136 listed in the FDA Orange Book. Original Data : FDA Website

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    Amneal Pharmaceuticals

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    01 AMNEAL PHARMS (2)

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    01 TABLET;SUBLINGUAL (2)

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    01 BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE (2)

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    BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; SUBLINGUAL
    EQ 2MG BASE;EQ 0.5...
    2013-02-22
    203136
    BUPRENORPHINE HYDR...
    RX
    No
    AB
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    US
    PHARMACOMPASS
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    your Marketing & Sales content
    Contact Supplier
    • FDA
    • EDQM
    • WHO-GMP
    Virtual Booth Upload your Marketing & Sales content on your company Virtual Booth, click HERE
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; SUBLINGUAL
    EQ 8MG BASE;EQ 2MG...
    2013-02-22
    203136
    BUPRENORPHINE HYDR...
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
    Upload
    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 203136

    Looking for FDA Orange Book APPLICATION 203136 2

    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 BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE, with a corresponding application number 203136.

    Regulatory Information RX

    With a dosage strength EQ 2MG BASE;EQ 0.5MG BASE

    Dosage Form Route TABLET; SUBLINGUAL

    Reference Listed Drug No

    Approved since 2013-02-22

    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 BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE, with a corresponding application number 203136.

    Regulatory Information RX

    With a dosage strength EQ 8MG BASE;EQ 2MG BASE

    Dosage Form Route TABLET; SUBLINGUAL

    Reference Listed Drug No

    Approved since 2013-02-22

    Therapeutic Equivalence (TE) Code AB

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