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    Halobetasol Propionate

    ACTIVE PHARMA INGREDIENTS

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    06 1MAYNE PHARMA

    07 4PADAGIS ISRAEL

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    01

    COSETTE

    U.S.A
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    COSETTE

    U.S.A
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    RLD : No

    TE Code : AB

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2005-06-14

    Application Number : 77109

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    COSETTE

    U.S.A
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    COSETTE

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    RLD : No

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2006-09-07

    Application Number : 77721

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    FOUGERA PHARMS

    U.S.A
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    RLD : No

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-12-16

    Application Number : 76903

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    FOUGERA PHARMS

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    RLD : No

    TE Code : AB

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-12-16

    Application Number : 77001

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    PADAGIS ISRAEL

    Israel
    CTAD25
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    PADAGIS ISRAEL

    Israel
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    RLD : No

    TE Code : AB

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-12-16

    Application Number : 76872

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    PADAGIS ISRAEL

    Israel
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    PADAGIS ISRAEL

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    RLD : No

    TE Code : AB

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-12-16

    Application Number : 77123

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    SUN PHARM INDS INC

    India
    CTAD25
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    SUN PHARM INDS INC

    India
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    RLD : Yes

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : ULTRAVATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1990-12-27

    Application Number : 19967

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    SUN PHARM INDS INC

    India
    CTAD25
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    SUN PHARM INDS INC

    India
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    CTAD25
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    RLD : Yes

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : ULTRAVATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1990-12-17

    Application Number : 19968

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    SUN PHARMA CANADA

    Country
    CTAD25
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    SUN PHARMA CANADA

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    RLD : No

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-12-16

    Application Number : 76994

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    SUN PHARMA CANADA

    Country
    CTAD25
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    SUN PHARMA CANADA

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    CTAD25
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    RLD : No

    TE Code :

    HALOBETASOL PROPIONATE

    Brand Name : HALOBETASOL PROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2005-08-04

    Application Number : 77227

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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