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    01 2DIPHENHYDRAMINE HYDROCHLORIDE

    02 1DOXYLAMINE SUCCINATE

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    Brand Name : DIPHENHYDRAMINE HYDR...

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    Regulatory Info : DISCN

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    DIPHENHYDRAMINE HYDROCHLORIDE

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    Dosage Form : CAPSULE;ORAL

    Brand Name : DIPHENHYDRAMINE HYDROCHLO...

    Dosage Strength : 25MG

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    Approval Date : 1983-01-27

    Application Number : 87977

    Regulatory Info : DISCN

    Registration Country : USA

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    Dosage Form : CAPSULE;ORAL

    Brand Name : DIPHENHYDRAMINE HYDROCHLO...

    Dosage Strength : 50MG

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    Approval Date : 1983-01-27

    Application Number : 87978

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    Brand Name : DOXYLAMINE SUCCINATE

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    DOXYLAMINE SUCCINATE

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    Dosage Form : TABLET;ORAL

    Brand Name : DOXYLAMINE SUCCINATE

    Dosage Strength : 25MG

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    Approval Date : 2004-08-27

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    Regulatory Info : OTC

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    IBUPROFEN

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    Dosage Form : TABLET;ORAL

    Brand Name : IBUPROFEN

    Dosage Strength : 200MG

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    Approval Date : 1999-03-01

    Application Number : 75010

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    IBUPROFEN

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    Dosage Form : TABLET;ORAL

    Brand Name : IBUPROFEN

    Dosage Strength : 200MG

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    Approval Date : 1999-03-01

    Application Number : 75139

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    IBUPROFEN

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    Dosage Form : TABLET;ORAL

    Brand Name : IBUPROFEN

    Dosage Strength : 100MG

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    Approval Date : 2004-06-17

    Application Number : 76741

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : LOPERAMIDE HYDROCHLO...

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    Regulatory Info : OTC

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    LOPERAMIDE HYDROCHLORIDE

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    Dosage Form : TABLET;ORAL

    Brand Name : LOPERAMIDE HYDROCHLORIDE

    Dosage Strength : 2MG

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    Approval Date : 2003-06-10

    Application Number : 76497

    Regulatory Info : OTC

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    Brand Name : METRONIDAZOLE

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    METRONIDAZOLE

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    Dosage Form : TABLET;ORAL

    Brand Name : METRONIDAZOLE

    Dosage Strength : 250MG

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    Approval Date : 1984-04-10

    Application Number : 19029

    Regulatory Info : DISCN

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    Brand Name : NAPROXEN SODIUM

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    Regulatory Info : OTC

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    NAPROXEN SODIUM

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    Dosage Form : TABLET;ORAL

    Brand Name : NAPROXEN SODIUM

    Dosage Strength : 220MG

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    Approval Date : 2017-01-23

    Application Number : 204872

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