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    Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.

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    Cefadroxil

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    01

    APOTHECON

    U.S.A
    RDD 2025
    Not Confirmed
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    APOTHECON

    U.S.A
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    APOTHECON

    U.S.A
    RDD 2025
    Not Confirmed
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    APOTHECON

    U.S.A
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    APOTHECON

    U.S.A
    RDD 2025
    Not Confirmed
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    APOTHECON

    U.S.A
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    SANDOZ

    Switzerland
    RDD 2025
    Not Confirmed
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    05

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    RDD 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50512

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    RDD 2025
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Approval Date : 1982-01-01

    Application Number : 50512

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    RDD 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    RDD 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    09

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
    arrow
    RDD 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    10

    WARNER CHILCOTT

    U.S.A
    RDD 2025
    Not Confirmed
    arrow

    WARNER CHILCOTT

    U.S.A
    arrow
    RDD 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50528

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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