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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    US WorldMeds

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    01 1DANTROLENE SODIUM

    02 1EFLORNITHINE HYDROCHLORIDE

    03 1LOFEXIDINE HYDROCHLORIDE

    04 1MELPHALAN HYDROCHLORIDE

    05 5NADOLOL

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    01

    Brand Name : REVONTO

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

    U.S.A
    2024 ACI Convention
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    RLD : No

    TE Code : AP

    DANTROLENE SODIUM

    US WorldMeds

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : REVONTO

    Dosage Strength : 20MG/VIAL

    Approval Date : 2007-07-24

    Application Number : 78378

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : IWILFIN

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

    U.S.A
    2024 ACI Convention
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    RLD : Yes

    TE Code :

    EFLORNITHINE HYDROCHLORIDE

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : IWILFIN

    Dosage Strength : EQ 192MG BASE

    Approval Date : 2023-12-13

    Application Number : 215500

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : LUCEMYRA

    U.S.A
    2024 ACI Convention
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    Brand Name : LUCEMYRA

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    RLD : Yes

    TE Code : AB

    LOFEXIDINE HYDROCHLORIDE

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : LUCEMYRA

    Dosage Strength : EQ 0.18MG BASE

    Approval Date : 2018-05-16

    Application Number : 209229

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    Brand Name : MELPHALAN HYDROCHLOR...

    U.S.A
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    Brand Name : MELPHALAN HYDROCHLOR...

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    RLD : No

    TE Code :

    MELPHALAN HYDROCHLORIDE

    US WorldMeds

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : MELPHALAN HYDROCHLORIDE

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2019-05-03

    Application Number : 207032

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : CORGARD

    U.S.A
    2024 ACI Convention
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    Brand Name : CORGARD

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    RLD : Yes

    TE Code :

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : CORGARD

    Dosage Strength : 40MG

    Approval Date : 1982-01-01

    Application Number : 18063

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    Brand Name : CORGARD

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    RLD : Yes

    TE Code :

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : CORGARD

    Dosage Strength : 80MG

    Approval Date : 1982-01-01

    Application Number : 18063

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    Brand Name : CORGARD

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

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    RLD : No

    TE Code :

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : CORGARD

    Dosage Strength : 120MG

    Approval Date : 1982-01-01

    Application Number : 18063

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    Brand Name : CORGARD

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

    U.S.A
    2024 ACI Convention
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    RLD : No

    TE Code :

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : CORGARD

    Dosage Strength : 160MG

    Approval Date : 1982-01-01

    Application Number : 18063

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : CORGARD

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

    U.S.A
    2024 ACI Convention
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    RLD : Yes

    TE Code :

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET; ORAL

    Proprietary Name : CORGARD

    Dosage Strength : 20MG

    Approval Date : 1986-10-28

    Application Number : 18063

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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