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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
    IMCAS Asia
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    ABRAXIS PHARM

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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
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    AM REGENT

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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
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    AM REGENT

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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
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    AM REGENT

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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
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    AM REGENT

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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
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    AM REGENT

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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
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    AM REGENT

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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
    IMCAS Asia
    Not Confirmed
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    NIVAGEN PHARMS INC

    U.S.A
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    IMCAS Asia
    Not Confirmed
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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
    IMCAS Asia
    Not Confirmed
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    NIVAGEN PHARMS INC

    U.S.A
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    IMCAS Asia
    Not Confirmed
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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
    IMCAS Asia
    Not Confirmed
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    NIVAGEN PHARMS INC

    U.S.A
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    IMCAS Asia
    Not Confirmed
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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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