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    Dosage Strength : 0.25%

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    Approval Date : 2020-10-26

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    Dosage Strength : 0.2%

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    Approval Date : 2024-12-13

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    Brand Name : LOTEMAX

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.5%

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    Approval Date : 1998-03-09

    Application Number : 20583

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    Brand Name : ALREX

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.2%

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    Approval Date : 1998-03-09

    Application Number : 20803

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    LOTEPREDNOL ETABONATE; TOBRAMYCIN

    Brand Name : ZYLET

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    Approval Date : 2004-12-14

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    LOTEPREDNOL ETABONATE

    Brand Name : LOTEMAX

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 0.5%

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    Approval Date : 2011-04-15

    Application Number : 200738

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    Brand Name : LOTEMAX

    Dosage Form : GEL;OPHTHALMIC

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    Approval Date : 2012-09-28

    Application Number : 202872

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    Brand Name : LOTEMAX SM

    Dosage Form : GEL;OPHTHALMIC

    Dosage Strength : 0.38%

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    Approval Date : 2019-02-22

    Application Number : 208219

    Regulatory Info : RX

    Registration Country : USA

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    Hikma Pharmaceuticals

    United Kingdom
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    Dosage Form : GEL;OPHTHALMIC

    Dosage Strength : 0.5%

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    Approval Date : 2023-11-29

    Application Number : 213956

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    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.2%

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    Approval Date : 2023-12-26

    Application Number : 215550

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    Lupin Ltd

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    Brand Name : LOTEPREDNOL ETABONATE

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    Approval Date : 2024-04-24

    Application Number : 215719

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    Padagis

    Israel
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    Approval Date : 2024-07-10

    Application Number : 215203

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    Padagis

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    Brand Name : LOTEPREDNOL ETABONATE

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.5%

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    Approval Date : 2025-01-29

    Application Number : 215204

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    Approval Date : 1998-03-09

    Application Number : 20841

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    Brand Name : LOTEPREDNOL ETABONATE

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    Approval Date : 2019-04-17

    Application Number : 207609

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    Approval Date : 2021-02-10

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    Brand Name : LOTEPREDNOL ETABONATE

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    Dosage Strength : 0.2%

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    Approval Date : 2023-04-12

    Application Number : 215933

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    Approval Date : 2021-02-26

    Application Number : 212450

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    Dosage Form : GEL;OPHTHALMIC

    Dosage Strength : 0.5%

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    Approval Date : 2023-08-09

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