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    Trimethoprim Sulfate

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    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : POLYTRIM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML

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    Approval Date : 1988-10-20

    Application Number : 50567

    Regulatory Info : DISCN

    Registration Country : USA

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    Canada
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    Regulatory Info : RX

    Registration Country : USA

    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML

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    Approval Date : 1997-02-14

    Application Number : 64120

    Regulatory Info : RX

    Registration Country : USA

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    Epic Pharma. LLC.

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    Regulatory Info : RX

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    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML

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    Approval Date : 1998-12-17

    Application Number : 65006

    Regulatory Info : RX

    Registration Country : USA

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    Regulatory Info : Prescription

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    Trimethoprim Sulfate

    Brand Name : PMS-POLYTRIMETHOPRIM

    Dosage Form : LIQUID

    Dosage Strength : 1MG/ML

    Packaging : 10ML

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    Regulatory Info : Prescription

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    Sandoz B2B

    Switzerland
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    Regulatory Info : RX

    Registration Country : USA

    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML

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    Approval Date : 1998-04-13

    Application Number : 64211

    Regulatory Info : RX

    Registration Country : USA

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    Somerset Pharmaceuticals Inc

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML

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    Approval Date : 2024-08-05

    Application Number : 211572

    Regulatory Info : RX

    Registration Country : USA

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