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    Trimethoprim Sulfate

    ACTIVE PHARMA INGREDIENTS

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    01 1ALLERGAN

    02 1BAUSCH AND LOMB

    03 1EPIC PHARMA LLC

    04 1SANDOZ

    05 1SOMERSET THERAPS LLC

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    ALLERGAN

    U.S.A
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    RLD : Yes

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    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : POLYTRIM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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

    Approval Date : 1988-10-20

    Application Number : 50567

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    BAUSCH AND LOMB

    Canada
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    BAUSCH AND LOMB

    Canada
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    RLD : No

    TE Code : AT

    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

    Approval Date : 1997-02-14

    Application Number : 64120

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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    03

    EPIC PHARMA LLC

    U.S.A
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    RLD : No

    TE Code : AT

    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

    Approval Date : 1998-12-17

    Application Number : 65006

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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    04

    SANDOZ

    Switzerland
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    SANDOZ

    Switzerland
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    RLD : No

    TE Code : AT

    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

    Approval Date : 1998-04-13

    Application Number : 64211

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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    05

    SOMERSET THERAPS LLC

    U.S.A
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    SOMERSET THERAPS LLC

    U.S.A
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    RLD : No

    TE Code : AT

    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

    Approval Date : 2024-08-05

    Application Number : 211572

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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