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    Cefadroxil

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    01 5ANI PHARMS

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    01

    APOTHECON

    U.S.A
    STLE Annual Meeting
    Not Confirmed
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    APOTHECON

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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
    STLE Annual Meeting
    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 :

    blank

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    03

    APOTHECON

    U.S.A
    STLE Annual Meeting
    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 :

    blank

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    04

    SANDOZ

    Switzerland
    STLE Annual Meeting
    Not Confirmed
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    05

    WARNER CHILCOTT

    U.S.A
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    STLE Annual Meeting
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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 :

    blank

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    06

    WARNER CHILCOTT

    U.S.A
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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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 :

    blank

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    07

    WARNER CHILCOTT

    U.S.A
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    STLE Annual Meeting
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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 :

    blank

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    08

    WARNER CHILCOTT

    U.S.A
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    STLE Annual Meeting
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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
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    STLE Annual Meeting
    Not Confirmed
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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
    STLE Annual Meeting
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    STLE Annual Meeting
    Not Confirmed
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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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