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    Anhydrous cefadroxil

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    Bristol Laboratories Ltd

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    Approval Date : 1982-08-31

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    Dosage Strength : EQ 125MG BASE/5ML

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    Approval Date : 1982-01-01

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    Bristol Myers Squibb

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    Bristol Myers Squibb

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    Dosage Strength : EQ 500MG BASE/5ML

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    Bristol Myers Squibb

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE

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    Approval Date : 1982-06-10

    Application Number : 62390

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    Switzerland
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    Dosage Strength : EQ 500MG BASE

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    Approval Date : 1982-01-01

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    Warner Chilcott Company, LLC

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    Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Warner Chilcott Company, LLC

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    Warner Chilcott Company, LLC

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    Dosage Strength : EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    Warner Chilcott Company, LLC

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    Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    Warner Chilcott Company, LLC

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

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    Approval Date : 1982-01-01

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    Warner Chilcott Company, LLC

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    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**

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    Approval Date : 1982-01-01

    Application Number : 50528

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