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    01 1CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

    02 3FENOPROFEN CALCIUM

    03 3KETOPROFEN

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    01

    Brand Name : CHLORDIAZEPOXIDE HYD...

    U.S.A
    Florida Innovation
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    Brand Name : CHLORDIAZEPOXIDE HYD...

    U.S.A
    Florida Innovation
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    RLD : No

    TE Code : AB

    CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CHLORDIAZEPOXIDE HYDROCH...

    Dosage Strength : 5MG;2.5MG

    Approval Date : 2020-07-29

    Application Number : 210579

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
    Not Confirmed
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    RLD : No

    TE Code :

    FENOPROFEN CALCIUM

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : FENOPROFEN CALCIUM

    Dosage Strength : EQ 200MG BASE

    Approval Date : 2023-05-16

    Application Number : 215548

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
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    RLD : No

    TE Code :

    FENOPROFEN CALCIUM

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : FENOPROFEN CALCIUM

    Dosage Strength : EQ 300MG BASE

    Approval Date : 2023-05-16

    Application Number : 215548

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    04

    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : FENOPROFEN CALCIUM

    U.S.A
    Florida Innovation
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    RLD : No

    TE Code :

    FENOPROFEN CALCIUM

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : FENOPROFEN CALCIUM

    Dosage Strength : EQ 400MG BASE

    Approval Date : 2023-05-16

    Application Number : 215548

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : KETOPROFEN

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : KETOPROFEN

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    Florida Innovation
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    RLD : No

    TE Code :

    KETOPROFEN

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : KETOPROFEN

    Dosage Strength : 25MG

    Approval Date : 1993-01-29

    Application Number : 74014

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

    blank

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    06

    Brand Name : KETOPROFEN

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : KETOPROFEN

    U.S.A
    Florida Innovation
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    RLD : No

    TE Code : AB

    KETOPROFEN

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : KETOPROFEN

    Dosage Strength : 50MG

    Approval Date : 1993-01-29

    Application Number : 74014

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : KETOPROFEN

    U.S.A
    Florida Innovation
    Not Confirmed
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    Brand Name : KETOPROFEN

    U.S.A
    Florida Innovation
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    • fda
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    • WHO-GMP
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    RLD : No

    TE Code :

    KETOPROFEN

    Misemer Pharmacetical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : KETOPROFEN

    Dosage Strength : 75MG

    Approval Date : 1993-01-29

    Application Number : 74014

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

    blank

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