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    Contract Pharmacal Corporation

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    01 2CETIRIZINE HYDROCHLORIDE

    02 2CIMETIDINE

    03 4FAMOTIDINE

    04 1FOLIC ACID

    05 9IBUPROFEN

    06 1IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

    07 1LOPERAMIDE HYDROCHLORIDE

    08 2NAPROXEN SODIUM

    09 1PREDNISONE

    10 1QUINIDINE SULFATE

    11 1RANITIDINE HYDROCHLORIDE

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    01

    Brand Name : CETIRIZINE HYDROCHLO...

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    Brand Name : CETIRIZINE HYDROCHLO...

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    Regulatory Info : OTC

    Registration Country : USA

    CETIRIZINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : CETIRIZINE HYDROCHLORIDE ...

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2007-12-27

    Application Number : 76047

    Regulatory Info : OTC

    Registration Country : USA

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    02

    Brand Name : CETIRIZINE HYDROCHLO...

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    Regulatory Info : OTC

    Registration Country : USA

    CETIRIZINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : CETIRIZINE HYDROCHLORIDE ...

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2007-12-27

    Application Number : 76047

    Regulatory Info : OTC

    Registration Country : USA

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    03

    Brand Name : CIMETIDINE

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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : CIMETIDINE

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 1998-06-19

    Application Number : 74961

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : CIMETIDINE

    Dosage Strength : 200MG

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    Approval Date : 1998-06-19

    Application Number : 74963

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : FAMOTIDINE

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    Regulatory Info : RX

    Registration Country : USA

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : FAMOTIDINE

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2023-12-20

    Application Number : 217669

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FAMOTIDINE

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    Regulatory Info : RX

    Registration Country : USA

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : FAMOTIDINE

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2023-12-20

    Application Number : 217669

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FAMOTIDINE

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    Regulatory Info : OTC

    Registration Country : USA

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : FAMOTIDINE

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2024-05-28

    Application Number : 218003

    Regulatory Info : OTC

    Registration Country : USA

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    Brand Name : FAMOTIDINE

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    Regulatory Info : OTC

    Registration Country : USA

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : FAMOTIDINE

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2024-05-28

    Application Number : 218003

    Regulatory Info : OTC

    Registration Country : USA

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    09

    Brand Name : FOLIC ACID

    U.S.A
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    Brand Name : FOLIC ACID

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    Regulatory Info : DISCN

    Registration Country : USA

    FOLIC ACID

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : FOLIC ACID

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85061

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Brand Name : IBUPROFEN

    U.S.A
    2024 ACI Convention
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    Brand Name : IBUPROFEN

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    Regulatory Info :

    Registration Country : USA

    IBUPROFEN

    Contract Pharmacal Corporation

    Dosage Form : TABLET;ORAL

    Brand Name : IBUPROFEN

    Dosage Strength : 800MG

    Packaging :

    Approval Date :

    Application Number : 72300

    Regulatory Info :

    Registration Country : USA

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