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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    01 2APRACLONIDINE HYDROCHLORIDE

    02 1CETIRIZINE HYDROCHLORIDE

    03 1CHLOROPROCAINE HYDROCHLORIDE

    04 2CYCLOSPORINE

    05 1DEXAMETHASONE

    06 1DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    07 1DEXAMETHASONE; TOBRAMYCIN

    08 1FLUOROMETHOLONE ACETATE

    09 1FLUOROMETHOLONE ACETATE; TOBRAMYCIN

    10 2MOXIFLOXACIN HYDROCHLORIDE

    11 1NATAMYCIN

    12 2NEPAFENAC

    13 1PREDNISOLONE ACETATE

    14 1RIMEXOLONE

    15 1TRIAMCINOLONE ACETONIDE

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    01

    Brand Name : IOPIDINE

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    Brand Name : IOPIDINE

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    Regulatory Info : RX

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    APRACLONIDINE HYDROCHLORIDE

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    Dosage Form : SOLUTION/DROPS;OPHTHALMI...

    Brand Name : IOPIDINE

    Dosage Strength : EQ 1% BASE

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    Approval Date : 1987-12-31

    Application Number : 19779

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : IOPIDINE

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    APRACLONIDINE HYDROCHLORIDE

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    Dosage Form : SOLUTION/DROPS;OPHTHALMI...

    Brand Name : IOPIDINE

    Dosage Strength : EQ 0.5% BASE

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    Approval Date : 1993-07-30

    Application Number : 20258

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : ZERVIATE

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    Regulatory Info : RX

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    CETIRIZINE HYDROCHLORIDE

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    Dosage Form : SOLUTION/DROPS;OPHTHALMI...

    Brand Name : ZERVIATE

    Dosage Strength : EQ 0.24% BASE

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    Approval Date : 2017-05-30

    Application Number : 208694

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : IHEEZO

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    Regulatory Info : RX

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    CHLOROPROCAINE HYDROCHLORIDE

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    Dosage Form : GEL;OPHTHALMIC

    Brand Name : IHEEZO

    Dosage Strength : 3%

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    Approval Date : 2022-09-27

    Application Number : 216227

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : VERKAZIA

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    CYCLOSPORINE

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    Dosage Form : EMULSION;OPHTHALMIC

    Brand Name : VERKAZIA

    Dosage Strength : 0.1%

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    Approval Date : 2021-06-23

    Application Number : 214965

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : VEVYE

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    Brand Name : VEVYE

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    CYCLOSPORINE

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    Dosage Form : SOLUTION;OPHTHALMIC

    Brand Name : VEVYE

    Dosage Strength : 0.1%

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    Approval Date : 2023-05-30

    Application Number : 217469

    Regulatory Info : RX

    Registration Country : USA

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    07

    Brand Name : MAXIDEX

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    Brand Name : MAXIDEX

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    Regulatory Info : RX

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    DEXAMETHASONE

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    Dosage Form : SUSPENSION/DROPS;OPHTHAL...

    Brand Name : MAXIDEX

    Dosage Strength : 0.1%

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    Approval Date : 1982-01-01

    Application Number : 13422

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : MAXITROL

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    Brand Name : MAXITROL

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    Regulatory Info : RX

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    DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

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    Dosage Form : SUSPENSION/DROPS;OPHTHAL...

    Brand Name : MAXITROL

    Dosage Strength : 0.1%;EQ 3.5MG BASE/ML;...

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50023

    Regulatory Info : RX

    Registration Country : USA

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    09

    Brand Name : TOBRADEX ST

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    Brand Name : TOBRADEX ST

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    Regulatory Info : RX

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    DEXAMETHASONE; TOBRAMYCIN

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    Dosage Form : SUSPENSION/DROPS;OPHTHAL...

    Brand Name : TOBRADEX ST

    Dosage Strength : 0.05%;0.3%

    Packaging :

    Approval Date : 2009-02-13

    Application Number : 50818

    Regulatory Info : RX

    Registration Country : USA

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    10

    Brand Name : FLAREX

    U.S.A
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    Brand Name : FLAREX

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    Regulatory Info : RX

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    FLUOROMETHOLONE ACETATE

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    Dosage Form : SUSPENSION/DROPS;OPHTHAL...

    Brand Name : FLAREX

    Dosage Strength : 0.1%

    Packaging :

    Approval Date : 1986-02-11

    Application Number : 19079

    Regulatory Info : RX

    Registration Country : USA

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