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

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Aminophylline

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    01

    FISONS

    United Kingdom
    Discovery on Target
    Not Confirmed
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    FISONS

    United Kingdom
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : SOMOPHYLLIN

    Dosage Form : ENEMA;RECTAL

    Dosage Strength : 300MG/5ML

    Approval Date : 1982-04-02

    Application Number : 18232

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    GD SEARLE LLC

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

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 2386

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    GD SEARLE LLC

    U.S.A
    Discovery on Target
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG

    Approval Date : 1982-01-01

    Application Number : 2386

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    HOSPIRA

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

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100MG/100ML

    Approval Date : 1984-12-12

    Application Number : 18924

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    HOSPIRA

    U.S.A
    Discovery on Target
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 200MG/100ML

    Approval Date : 1984-12-12

    Application Number : 18924

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    HOSPIRA

    U.S.A
    Discovery on Target
    Not Confirmed
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    HOSPIRA

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

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 400MG/100ML

    Approval Date : 1984-12-12

    Application Number : 18924

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    HOSPIRA

    U.S.A
    Discovery on Target
    Not Confirmed
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    HOSPIRA

    U.S.A
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    Discovery on Target
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/100ML

    Approval Date : 1984-12-12

    Application Number : 18924

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    TEVA PARENTERAL

    Israel
    Discovery on Target
    Not Confirmed
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    TEVA PARENTERAL

    Israel
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Approval Date : 1991-09-25

    Application Number : 81142

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    VALE

    Country
    Discovery on Target
    Not Confirmed
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    VALE

    Country
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    Not Confirmed
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 200MG

    Approval Date : 1982-01-01

    Application Number : 84530

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    VALE

    Country
    Discovery on Target
    Not Confirmed
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    VALE

    Country
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code :

    AMINOPHYLLINE

    Brand Name : AMINOPHYLLINE

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 84531

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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