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    TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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    Your reliable CDMO partner - agile, scalable, top-quality Small Molecule API & HPAPI solutions from concept to market

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

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    Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.

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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
    CPhI India
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    Brand Name : BAXDELA

    U.S.A
    CPhI India
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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
    CPhI India
    Not Confirmed
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    Brand Name : BAXDELA

    U.S.A
    CPhI India
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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
    CPhI India
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    Brand Name : ORBACTIV

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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
    CPhI India
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    Brand Name : KIMYRSA

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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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