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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Levonordefrin

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1BELMORA LLC

    02 1DENTSPLY PHARM

    03 1DEPROCO

    04 2EASTMAN KODAK

    05 1SEPTODONT

    06 1SOLVAY

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    01

    BELMORA LLC

    U.S.A
    Antibody Engineering
    Not Confirmed
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    BELMORA LLC

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : MEPIVACAINE HYDROCHLORIDE W/ LEVONORDEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1983-10-21

    Application Number : 84850

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    DENTSPLY PHARM

    U.S.A
    Antibody Engineering
    Not Confirmed
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    DENTSPLY PHARM

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : POLOCAINE W/ LEVONORDEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1988-04-14

    Application Number : 89517

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    EASTMAN KODAK

    U.S.A
    Antibody Engineering
    Not Confirmed
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    EASTMAN KODAK

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    LEVONORDEFRIN; PROCAINE HYDROCHLORIDE; PROPOXYCAINE HYDROCHLORIDE

    Brand Name : RAVOCAINE AND NOVOCAIN W/ NEO-COBEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%;0.4%

    Approval Date : 1982-01-01

    Application Number : 8592

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    EASTMAN KODAK

    U.S.A
    Antibody Engineering
    Not Confirmed
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    EASTMAN KODAK

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : CARBOCAINE W/ NEO-COBEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1982-01-01

    Application Number : 12125

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    SEPTODONT

    U.S.A
    Antibody Engineering
    Not Confirmed
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    SEPTODONT

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : ISOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1982-01-01

    Application Number : 84697

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    DEPROCO

    U.S.A
    Antibody Engineering
    Not Confirmed
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    DEPROCO

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : SCANDONEST L

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1984-10-10

    Application Number : 88388

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    SOLVAY

    Belgium
    Antibody Engineering
    Not Confirmed
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    SOLVAY

    Belgium
    arrow
    Antibody Engineering
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

    Brand Name : ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.05MG/ML;2%

    Approval Date : 1982-01-01

    Application Number : 85010

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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