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    Alclometasone Dipropionate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 4FOUGERA PHARMS

    02 2GLENMARK PHARMS LTD

    03 2TARO

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    01

    FOUGERA PHARMS

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    FOUGERA PHARMS

    U.S.A
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    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ACLOVATE

    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    Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1982-12-14

    Application Number : 18702

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    FOUGERA PHARMS

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    FOUGERA PHARMS

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ACLOVATE

    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    Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1982-12-14

    Application Number : 18707

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    FOUGERA PHARMS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    FOUGERA PHARMS

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2005-07-18

    Application Number : 76884

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    FOUGERA PHARMS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    FOUGERA PHARMS

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2005-07-12

    Application Number : 76973

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    GLENMARK PHARMS LTD

    India
    The Generic Rx Session
    Not Confirmed
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    GLENMARK PHARMS LTD

    India
    arrow
    The Generic Rx Session
    Not Confirmed
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2009-06-23

    Application Number : 79061

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    GLENMARK PHARMS LTD

    India
    The Generic Rx Session
    Not Confirmed
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    GLENMARK PHARMS LTD

    India
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2009-07-30

    Application Number : 79227

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    TARO

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    TARO

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2005-09-15

    Application Number : 76587

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    TARO

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    TARO

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    ALCLOMETASONE DIPROPIONATE

    Brand Name : ALCLOMETASONE DIPROPIONATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Approval Date : 2004-07-29

    Application Number : 76730

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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