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    Melinta Therapeutics

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    01 2DELAFLOXACIN MEGLUMINE

    02 2ORITAVANCIN DIPHOSPHATE

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    Brand Name : BAXDELA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BAXDELA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    RLD : Yes

    TE Code :

    DELAFLOXACIN MEGLUMINE

    Melinta Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : BAXDELA

    Dosage Strength : EQ 450MG BASE

    Approval Date : 2017-06-19

    Application Number : 208610

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : BAXDELA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Brand Name : BAXDELA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code :

    DELAFLOXACIN MEGLUMINE

    Melinta Therapeutics

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : BAXDELA

    Dosage Strength : EQ 300MG BASE/VIAL

    Approval Date : 2017-06-19

    Application Number : 208611

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : ORBACTIV

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : ORBACTIV

    U.S.A
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    RLD : Yes

    TE Code :

    ORITAVANCIN DIPHOSPHATE

    Melinta Therapeutics

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : ORBACTIV

    Dosage Strength : EQ 400MG BASE/VIAL

    Approval Date : 2014-08-06

    Application Number : 206334

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : KIMYRSA

    U.S.A
    Pharmtech & Ingredients
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    Brand Name : KIMYRSA

    U.S.A
    Pharmtech & Ingredients
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    • fda
    • EDQM
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    RLD : Yes

    TE Code :

    ORITAVANCIN DIPHOSPHATE

    Melinta Therapeutics

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : KIMYRSA

    Dosage Strength : EQ 1.2GM BASE/VIAL

    Approval Date : 2021-03-12

    Application Number : 214155

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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