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    InvaTech Pharma Solutions LLC

    EVENTS

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    01 2BUPROPION HYDROCHLORIDE

    02 3DIVALPROEX SODIUM

    03 1FLUOCINOLONE ACETONIDE

    04 2GABAPENTIN

    05 1MECLIZINE HYDROCHLORIDE

    06 1METHYLPREDNISOLONE

    07 3PROMETHAZINE HYDROCHLORIDE

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    01

    Brand Name : BUPROPION HYDROCHLOR...

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : BUPROPION HYDROCHLOR...

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    RLD : No

    TE Code :

    BUPROPION HYDROCHLORIDE

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 100MG

    Approval Date : 2000-10-10

    Application Number : 75613

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : BUPROPION HYDROCHLOR...

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : BUPROPION HYDROCHLOR...

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    RLD : No

    TE Code :

    BUPROPION HYDROCHLORIDE

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 75MG

    Approval Date : 2000-10-10

    Application Number : 75613

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : DIVALPROEX SODIUM

    U.S.A
    2024 ACI Convention
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    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 500MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78290

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : DIVALPROEX SODIUM

    U.S.A
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    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 250MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78290

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : DIVALPROEX SODIUM

    U.S.A
    2024 ACI Convention
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    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 125MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78290

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : FLUOCINOLONE ACETONI...

    U.S.A
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    Brand Name : FLUOCINOLONE ACETONI...

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    RLD : No

    TE Code :

    FLUOCINOLONE ACETONIDE

    InvaTech Pharma Solutions LLC

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : FLUOCINOLONE ACETONIDE

    Dosage Strength : 0.025%

    Approval Date : 1982-12-16

    Application Number : 88045

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : GABAPENTIN

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : GABAPENTIN

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    RLD : No

    TE Code :

    GABAPENTIN

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : GABAPENTIN

    Dosage Strength : 600MG

    Approval Date : 2006-07-06

    Application Number : 76877

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    Brand Name : GABAPENTIN

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : GABAPENTIN

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    2024 ACI Convention
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    RLD : No

    TE Code :

    GABAPENTIN

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : GABAPENTIN

    Dosage Strength : 800MG

    Approval Date : 2006-07-06

    Application Number : 76877

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : MECLIZINE HYDROCHLOR...

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : MECLIZINE HYDROCHLOR...

    U.S.A
    2024 ACI Convention
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    RLD : No

    TE Code : AA

    MECLIZINE HYDROCHLORIDE

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : MECLIZINE HYDROCHLORIDE

    Dosage Strength : 25MG

    Approval Date : 1989-05-22

    Application Number : 84092

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    10

    Brand Name : METHYLPREDNISOLONE

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : METHYLPREDNISOLONE

    U.S.A
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    RLD : No

    TE Code :

    METHYLPREDNISOLONE

    InvaTech Pharma Solutions LLC

    Dosage Form : TABLET; ORAL

    Proprietary Name : METHYLPREDNISOLONE

    Dosage Strength : 4MG

    Approval Date : 1982-01-01

    Application Number : 87341

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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