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    Key Therapeutics

    EVENTS

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    DIGITAL CONTENT

    FINISHED DOSAGE FORMULATIONS

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    01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    02 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE

    03 1CIPROFLOXACIN HYDROCHLORIDE

    04 1DEXAMETHASONE

    05 4FENOPROFEN CALCIUM

    06 1VORAPAXAR SULFATE

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    01

    Brand Name : BUTALBITAL, ACETAMIN...

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    2024 ACI Convention
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    Brand Name : BUTALBITAL, ACETAMIN...

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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Key Therapeutics

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 300MG;50MG;40MG

    Approval Date : 2017-08-04

    Application Number : 206615

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : TREZIX

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    Brand Name : TREZIX

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    RLD : No

    TE Code :

    ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE

    Key Therapeutics

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : TREZIX

    Dosage Strength : 320.5MG;30MG;16MG

    Approval Date : 2014-11-26

    Application Number : 204785

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : CETRAXAL

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    RLD : Yes

    TE Code :

    CIPROFLOXACIN HYDROCHLORIDE

    Key Therapeutics

    Dosage Form : SOLUTION/DROPS; OTIC

    Proprietary Name : CETRAXAL

    Dosage Strength : EQ 0.2% BASE

    Approval Date : 2009-05-01

    Application Number : 21918

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : DEXAMETHASONE

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    RLD : No

    TE Code :

    DEXAMETHASONE

    Key Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : DEXAMETHASONE

    Dosage Strength : 1.5MG

    Approval Date : 1983-04-28

    Application Number : 88237

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : NALFON

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    RLD : No

    TE Code :

    FENOPROFEN CALCIUM

    Key Therapeutics

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : NALFON

    Dosage Strength : EQ 300MG BASE **Federal ...

    Approval Date : 1982-01-01

    Application Number : 17604

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : NALFON

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    RLD : Yes

    TE Code :

    FENOPROFEN CALCIUM

    Key Therapeutics

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : NALFON

    Dosage Strength : EQ 200MG BASE

    Approval Date : 1982-01-01

    Application Number : 17604

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    Brand Name : NALFON

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    RLD : Yes

    TE Code :

    FENOPROFEN CALCIUM

    Key Therapeutics

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : NALFON

    Dosage Strength : EQ 400MG BASE

    Approval Date : 2009-07-21

    Application Number : 17604

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    Brand Name : FENOPROFEN CALCIUM

    U.S.A
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    RLD : No

    TE Code :

    FENOPROFEN CALCIUM

    Key Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : FENOPROFEN CALCIUM

    Dosage Strength : EQ 600MG BASE

    Approval Date : 1988-08-17

    Application Number : 72267

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : ZONTIVITY

    U.S.A
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    Brand Name : ZONTIVITY

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    RLD : Yes

    TE Code :

    VORAPAXAR SULFATE

    Key Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : ZONTIVITY

    Dosage Strength : EQ 2.08MG BASE

    Approval Date : 2014-05-08

    Application Number : 204886

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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