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    Diphenhydramine Citrate

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    01 1Aurobindo Pharma Limited

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    Aurobindo Pharma Limited

    India
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    Aurobindo Pharma Limited

    India
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    Regulatory Info : OTC

    Registration Country : USA

    DIPHENHYDRAMINE CITRATE; IBUPROFEN

    Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 38MG;200MG

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    Approval Date : 2022-05-31

    Application Number : 216204

    Regulatory Info : OTC

    Registration Country : USA

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    Haleon

    United Kingdom
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    Regulatory Info : OTC

    Registration Country : USA

    DIPHENHYDRAMINE CITRATE; IBUPROFEN

    Brand Name : ADVIL PM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 38MG;200MG

    Packaging :

    Approval Date : 2005-12-21

    Application Number : 21394

    Regulatory Info : OTC

    Registration Country : USA

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    Perrigo Company plc

    Ireland
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    Regulatory Info : OTC

    Registration Country : USA

    DIPHENHYDRAMINE CITRATE; IBUPROFEN

    Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 38MG;200MG

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    Approval Date : 2008-12-22

    Application Number : 79113

    Regulatory Info : OTC

    Registration Country : USA

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    PLD ACQUISITIONS

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    Regulatory Info : OTC

    Registration Country : USA

    DIPHENHYDRAMINE CITRATE; IBUPROFEN

    Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 38MG;200MG

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    Approval Date : 2024-04-11

    Application Number : 211404

    Regulatory Info : OTC

    Registration Country : USA

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    XYZ Pharma

    Gabon
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    Regulatory Info : OTC

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    DIPHENHYDRAMINE CITRATE; IBUPROFEN

    Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 38MG;200MG

    Packaging :

    Approval Date : 2009-07-08

    Application Number : 90619

    Regulatory Info : OTC

    Registration Country : USA

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