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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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    Cefadroxil

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    ANI Pharmaceuticals Inc

    U.S.A
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    Approval Date : 1989-03-01

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    ANI Pharmaceuticals Inc

    U.S.A
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    Brand Name : CEFADROXIL

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    Approval Date : 1989-03-01

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    ANI Pharmaceuticals Inc

    U.S.A
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    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

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    Approval Date : 1989-03-01

    Application Number : 62698

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    Bristol Laboratories Ltd

    United Kingdom
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    Brand Name : ULTRACEF

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    Dosage Strength : EQ 125MG BASE/5ML

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    Approval Date : 1982-03-16

    Application Number : 62376

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    09

    Bristol Laboratories Ltd

    United Kingdom
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : ULTRACEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

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    Approval Date : 1982-03-16

    Application Number : 62376

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    10

    Bristol Laboratories Ltd

    United Kingdom
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : ULTRACEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

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    Approval Date : 1982-03-16

    Application Number : 62376

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    11

    Bristol Laboratories Ltd

    United Kingdom
    AACR Annual meeting
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    United Kingdom
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : ULTRACEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

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    Approval Date : 1982-03-16

    Application Number : 62378

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    Registration Country : USA

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    12

    Bristol Laboratories Ltd

    United Kingdom
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    Bristol Laboratories Ltd

    United Kingdom
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    AACR Annual meeting
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : ULTRACEF

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE

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    Approval Date : 1982-08-31

    Application Number : 62408

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Bristol Myers Squibb

    U.S.A
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62334

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Bristol Myers Squibb

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

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    Approval Date : 1982-01-01

    Application Number : 62334

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Bristol Myers Squibb

    U.S.A
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    U.S.A
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

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    Approval Date : 1982-01-01

    Application Number : 62334

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Bristol Myers Squibb

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    AACR Annual meeting
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : ULTRACEF

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE

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    Approval Date : 1982-06-10

    Application Number : 62390

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    IVAX Pharmaceuticals Inc

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1987-03-03

    Application Number : 62766

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    PUREPAC PHARM

    U.S.A
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    U.S.A
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    AACR Annual meeting
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    Regulatory Info : DISCN

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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1989-01-05

    Application Number : 63017

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sandoz B2B

    Switzerland
    AACR Annual meeting
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    AACR Annual meeting
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62291

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Sun Pharmaceutical Industries Limit...

    India
    AACR Annual meeting
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    AACR Annual meeting
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    Regulatory Info : DISCN

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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1999-06-22

    Application Number : 65015

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Sun Pharmaceutical Industries Limit...

    India
    AACR Annual meeting
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    Regulatory Info : DISCN

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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE

    Packaging :

    Approval Date : 1999-04-23

    Application Number : 65018

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Sun Pharmaceutical Industries Limit...

    India
    AACR Annual meeting
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML

    Packaging :

    Approval Date : 2003-03-26

    Application Number : 65115

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
    AACR Annual meeting
    Not Confirmed
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    Israel
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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1989-02-10

    Application Number : 62695

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Teva Pharmaceutical Industries

    Israel
    AACR Annual meeting
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1GM BASE

    Packaging :

    Approval Date : 1987-04-08

    Application Number : 62774

    Regulatory Info : RX

    Registration Country : USA

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    25

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Warner Chilcott Company, LLC

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50512

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50512

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Warner Chilcott Company, LLC

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50527

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Warner Chilcott Company, LLC

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50527

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Warner Chilcott Company, LLC

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50527

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Warner Chilcott Company, LLC

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Warner Chilcott Company, LLC

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50528

    Regulatory Info : DISCN

    Registration Country : USA

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