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

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    Triprolidine Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1ALPHARMA US PHARMS

    02 1ANIMA

    03 3CENCI

    04 1CHARTWELL RX

    05 4GLAXOSMITHKLINE

    06 1HALSEY

    07 1IVAX SUB TEVA PHARMS

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    09 2NEWTRON PHARMS

    10 1PHARM ASSOC

    11 1PVT FORM

    12 1SANDOZ

    13 1SUPERPHARM

    14 1TEVA

    15 2USL PHARMA

    16 1VITARINE

    17 2WATSON LABS

    18 1WEST WARD

    19 1WOCKHARDT

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    01

    WATSON LABS

    Ireland
    Discovery on Target
    Not Confirmed
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    WATSON LABS

    Ireland
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    Not Confirmed
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    RLD : No

    TE Code :

    TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

    Approval Date : 1982-01-01

    Application Number : 85094

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    ALPHARMA US PHARMS

    Ireland
    Discovery on Target
    Not Confirmed
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    ALPHARMA US PHARMS

    Ireland
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    Not Confirmed
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    RLD : No

    TE Code :

    TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE HYDROCHLORIDE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 1.25MG/5ML

    Approval Date : 1982-01-01

    Application Number : 85940

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    TRIPROLIDINE HYDROCHLORIDE

    Brand Name : ACTIDIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

    Approval Date : 1983-07-01

    Application Number : 11110

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    TRIPROLIDINE HYDROCHLORIDE

    Brand Name : ACTIDIL

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 1.25MG/5ML

    Approval Date : 1983-07-01

    Application Number : 11496

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

    Brand Name : ACTIFED W/ CODEINE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 10MG/5ML;30MG/5ML;1.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1984-04-04

    Application Number : 12575

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

    Brand Name : ACTIFED

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 120MG;5MG

    Approval Date : 1985-06-17

    Application Number : 18996

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    IVAX SUB TEVA PHARMS

    U.S.A
    Discovery on Target
    Not Confirmed
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    IVAX SUB TEVA PHARMS

    U.S.A
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    RLD : No

    TE Code :

    PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 60MG;2.5MG

    Approval Date : 1984-12-12

    Application Number : 85273

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    KV PHARM

    U.S.A
    Discovery on Target
    Not Confirmed
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    KV PHARM

    U.S.A
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    RLD : No

    TE Code :

    PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDES

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 120MG;5MG

    Approval Date : 1989-03-16

    Application Number : 71798

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    KV PHARM

    U.S.A
    Discovery on Target
    Not Confirmed
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    KV PHARM

    U.S.A
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDES

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 120MG;5MG

    Approval Date : 1991-11-25

    Application Number : 72758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    VITARINE

    Country
    Discovery on Target
    Not Confirmed
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    VITARINE

    Country
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    TRIPROLIDINE HYDROCHLORIDE

    Brand Name : TRIPROLIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

    Approval Date : 1982-01-01

    Application Number : 85610

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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