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    01 6GLAXO GRP LTD

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    01

    GLAXOSMITHKLINE

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    RLD : No

    TE Code :

    SALMETEROL XINAFOATE

    Brand Name : SEREVENT

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : EQ 0.021MG BASE/INH

    Approval Date : 1994-02-04

    Application Number : 20236

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    GLAXOSMITHKLINE

    United Kingdom
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    GLAXOSMITHKLINE

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    RLD : Yes

    TE Code :

    SALMETEROL XINAFOATE

    Brand Name : SEREVENT

    Dosage Form : POWDER;INHALATION

    Dosage Strength : EQ 0.05MG BASE/INH

    Approval Date : 1997-09-19

    Application Number : 20692

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    GLAXO GRP LTD

    United Kingdom
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    GLAXO GRP LTD

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    RLD : Yes

    TE Code : AB

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR DISKUS 100/50

    Dosage Form : POWDER;INHALATION

    Dosage Strength : 0.1MG/INH;EQ 0.05MG BASE/INH

    Approval Date : 2000-08-24

    Application Number : 21077

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    GLAXO GRP LTD

    United Kingdom
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    RLD : Yes

    TE Code : AB

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR DISKUS 250/50

    Dosage Form : POWDER;INHALATION

    Dosage Strength : 0.25MG/INH;EQ 0.05MG BASE/INH

    Approval Date : 2000-08-24

    Application Number : 21077

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    GLAXO GRP LTD

    United Kingdom
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    GLAXO GRP LTD

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    RLD : Yes

    TE Code : AB

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR DISKUS 500/50

    Dosage Form : POWDER;INHALATION

    Dosage Strength : 0.5MG/INH;EQ 0.05MG BASE/INH

    Approval Date : 2000-08-24

    Application Number : 21077

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    GLAXO GRP LTD

    United Kingdom
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    GLAXO GRP LTD

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    RLD : Yes

    TE Code :

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR HFA

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : 0.045MG/INH;EQ 0.021MG BASE/INH

    Approval Date : 2006-06-08

    Application Number : 21254

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    07

    GLAXO GRP LTD

    United Kingdom
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    GLAXO GRP LTD

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    RLD : Yes

    TE Code :

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR HFA

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : 0.115MG/INH;EQ 0.021MG BASE/INH

    Approval Date : 2006-06-08

    Application Number : 21254

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    08

    GLAXO GRP LTD

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    GLAXO GRP LTD

    United Kingdom
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    RLD : Yes

    TE Code :

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : ADVAIR HFA

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : 0.23MG/INH;EQ 0.021MG BASE/INH

    Approval Date : 2006-06-08

    Application Number : 21254

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    09

    HIKMA

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AB

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

    Dosage Form : POWDER;INHALATION

    Dosage Strength : 0.1MG/INH;EQ 0.05MG BASE/INH

    Approval Date : 2020-12-17

    Application Number : 203433

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    HIKMA

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AB

    FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE

    Brand Name : FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE

    Dosage Form : POWDER;INHALATION

    Dosage Strength : 0.25MG/INH;EQ 0.05MG BASE/INH

    Approval Date : 2020-12-17

    Application Number : 203433

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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