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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    01 1ATROPINE SULFATE

    02 1CALCIUM CHLORIDE

    03 6SODIUM CHLORIDE

    04 5STERILE WATER FOR INJECTION

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    01

    Brand Name : ATROPINE SULFATE

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    Brand Name : ATROPINE SULFATE

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    RLD : No

    TE Code : AP

    ATROPINE SULFATE

    Medefil

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : ATROPINE SULFATE

    Dosage Strength : 1MG/10ML (0.1MG/ML)

    Approval Date : 2022-11-04

    Application Number : 214970

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : CALCIUM CHLORIDE 10%

    U.S.A
    2024 ACI Convention
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    Brand Name : CALCIUM CHLORIDE 10%

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    RLD : No

    TE Code : AP

    CALCIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CALCIUM CHLORIDE 10%

    Dosage Strength : 100MG/ML

    Approval Date : 2019-05-01

    Application Number : 211553

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : SODIUM CHLORIDE 0.9%

    U.S.A
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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 9MG/ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    Brand Name : SODIUM CHLORIDE 0.9%

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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 18MG/2ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    Brand Name : SODIUM CHLORIDE 0.9%

    U.S.A
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    Brand Name : SODIUM CHLORIDE 0.9%

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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 22.5MG/2.5ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    Brand Name : SODIUM CHLORIDE 0.9%

    U.S.A
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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 27MG/3ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    Brand Name : SODIUM CHLORIDE 0.9%

    U.S.A
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    Brand Name : SODIUM CHLORIDE 0.9%

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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 45MG/5ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    Brand Name : SODIUM CHLORIDE 0.9%

    U.S.A
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    Not Confirmed
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    Brand Name : SODIUM CHLORIDE 0.9%

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    RLD : Yes

    TE Code :

    SODIUM CHLORIDE

    Medefil

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM CHLORIDE 0.9%

    Dosage Strength : 90MG/10ML (9MG/ML)

    Approval Date : 2012-01-06

    Application Number : 202832

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    09

    Brand Name : STERILE WATER FOR IN...

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : STERILE WATER FOR IN...

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    RLD : No

    TE Code :

    STERILE WATER FOR INJECTION

    Medefil

    Dosage Form : LIQUID; N/A

    Proprietary Name : STERILE WATER FOR INJECT...

    Dosage Strength : 100% (1ML)

    Approval Date : 2019-12-02

    Application Number : 211188

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    Brand Name : STERILE WATER FOR IN...

    U.S.A
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    RLD : No

    TE Code :

    STERILE WATER FOR INJECTION

    Medefil

    Dosage Form : LIQUID; N/A

    Proprietary Name : STERILE WATER FOR INJECT...

    Dosage Strength : 100% (2.5ML)

    Approval Date : 2019-12-02

    Application Number : 211188

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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