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    Pramoxine HCl

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1FERNDALE LABS

    02 1GENUS

    03 2MYLAN SPECIALITY LP

    04 4SEBELA IRELAND LTD

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    01

    FERNDALE LABS

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    FERNDALE LABS

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PRAMOSONE

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 0.5%;1%

    Approval Date : 1982-01-01

    Application Number : 83213

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    GENUS

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    GENUS

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1%

    Dosage Form : AEROSOL, METERED;TOPICAL

    Dosage Strength : 1%;1%

    Approval Date : 1988-05-17

    Application Number : 89440

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    SEBELA IRELAND LTD

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    SEBELA IRELAND LTD

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PRAMOSONE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.5%;1%

    Approval Date : 1982-01-01

    Application Number : 83778

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    04

    SEBELA IRELAND LTD

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    SEBELA IRELAND LTD

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PRAMOSONE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%;1%

    Approval Date : 1982-01-01

    Application Number : 85368

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    05

    SEBELA IRELAND LTD

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    SEBELA IRELAND LTD

    U.S.A
    arrow
    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PRAMOSONE

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 2.5%;1%

    Approval Date : 1982-01-01

    Application Number : 85979

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    06

    SEBELA IRELAND LTD

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    SEBELA IRELAND LTD

    U.S.A
    arrow
    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PRAMOSONE

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 1%;1%

    Approval Date : 1982-01-01

    Application Number : 85980

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    07

    MYLAN SPECIALITY LP

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    MYLAN SPECIALITY LP

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code : BX

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : PROCTOFOAM HC

    Dosage Form : AEROSOL, METERED;TOPICAL

    Dosage Strength : 1%;1%

    Approval Date : 1982-01-01

    Application Number : 86195

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : BX

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    08

    MYLAN SPECIALITY LP

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
    arrow

    MYLAN SPECIALITY LP

    U.S.A
    arrow
    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : BX

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Brand Name : EPIFOAM

    Dosage Form : AEROSOL, METERED;TOPICAL

    Dosage Strength : 1%;1%

    Approval Date : 1982-01-01

    Application Number : 86457

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : BX

    blank

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