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    Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

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    01 1ABRAXIS PHARM

    02 6AM REGENT

    03 2APOTEX

    04 3ASPIRO

    05 3FRESENIUS KABI USA

    06 3GLAND

    07 3NIVAGEN PHARMS INC

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    01

    ABRAXIS PHARM

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    The Battery Show Europe
    Not Confirmed
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    RLD : No

    TE Code :

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG ZINC/ML

    Approval Date : 1987-05-05

    Application Number : 19229

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
    Not Confirmed
    • fda
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    RLD : Yes

    TE Code :

    CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

    Brand Name : TRALEMENT

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (1ML)

    Approval Date : 2020-07-02

    Application Number : 209376

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
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    RLD : Yes

    TE Code :

    CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

    Brand Name : TRALEMENT

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (5ML)

    Approval Date : 2020-12-02

    Application Number : 209376

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
    Not Confirmed
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    RLD : Yes

    TE Code :

    CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

    Brand Name : MULTRYS

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 60MCG COPPER/ML;EQ 3MCG BASE/ML;EQ 6MCG SELENIUM/ML;EQ 1000MCG BASE/ML (1ML)

    Approval Date : 2021-06-30

    Application Number : 209376

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    05

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
    Not Confirmed
    • fda
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    RLD : Yes

    TE Code : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)

    Approval Date : 2019-07-18

    Application Number : 209377

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    06

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
    Not Confirmed
    • fda
    • EDQM
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    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 : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)

    Approval Date : 2019-07-18

    Application Number : 209377

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    07

    AM REGENT

    U.S.A
    The Battery Show Europe
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Battery Show Europe
    Not Confirmed
    • fda
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    RLD : Yes

    TE Code : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)

    Approval Date : 2020-04-15

    Application Number : 209377

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    08

    NIVAGEN PHARMS INC

    U.S.A
    The Battery Show Europe
    Not Confirmed
    arrow

    NIVAGEN PHARMS INC

    U.S.A
    arrow
    The Battery Show Europe
    Not Confirmed
    • fda
    • EDQM
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    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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    Flag U.S.A
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    RLD : No

    TE Code : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)

    Approval Date : 2024-07-05

    Application Number : 214597

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    09

    NIVAGEN PHARMS INC

    U.S.A
    The Battery Show Europe
    Not Confirmed
    arrow

    NIVAGEN PHARMS INC

    U.S.A
    arrow
    The Battery Show Europe
    Not Confirmed
    • 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 : No

    TE Code : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)

    Approval Date : 2024-07-05

    Application Number : 214597

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    NIVAGEN PHARMS INC

    U.S.A
    The Battery Show Europe
    Not Confirmed
    arrow

    NIVAGEN PHARMS INC

    U.S.A
    arrow
    The Battery Show Europe
    Not Confirmed
    • 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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    Flag U.S.A
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    RLD : No

    TE Code : AP

    ZINC SULFATE

    Brand Name : ZINC SULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)

    Approval Date : 2024-07-05

    Application Number : 214597

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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