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    05 2B. Braun Medical

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    07 3Caplin Point Laboratories Limited

    08 3Fresenius Kabi AB Brunna

    09 3Fresenius Kabi USA

    10 3Hospira, Inc.

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    12 1Lukare medical

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    01

    Abbott Laboratories

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Abbott Laboratories

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 3.5% M IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 3.5%;32MG/100ML;128MG/100ML;222MG/100ML;49MG/100ML

    Packaging :

    Approval Date : 1986-10-16

    Application Number : 19493

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Abbott Laboratories

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Packaging :

    Approval Date : 1986-12-16

    Application Number : 19564

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Abbott Laboratories

    U.S.A
    Nutri Ingredients Summit
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4.25%;10GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Packaging :

    Approval Date : 1986-12-16

    Application Number : 19564

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Abbott Laboratories

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Abbott Laboratories

    U.S.A
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Packaging :

    Approval Date : 1988-09-08

    Application Number : 19712

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    American Regent

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    American Regent

    U.S.A
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    Nutri Ingredients Summit
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2024-06-21

    Application Number : 218314

    Regulatory Info : RX

    Registration Country : USA

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    06

    American Regent

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    American Regent

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2024-06-21

    Application Number : 218314

    Regulatory Info : RX

    Registration Country : USA

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    07

    American Regent

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    American Regent

    U.S.A
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    Nutri Ingredients Summit
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2024-06-21

    Application Number : 218314

    Regulatory Info : RX

    Registration Country : USA

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    08

    B. Braun Medical

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    B. Braun Medical

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : ISOLYTE S PH 7.4 IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

    Packaging :

    Approval Date : 1984-04-04

    Application Number : 19006

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    B. Braun Medical

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    B. Braun Medical

    U.S.A
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : ISOLYTE S PH 7.4 IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

    Packaging :

    Approval Date : 1989-09-29

    Application Number : 19696

    Regulatory Info : RX

    Registration Country : USA

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    10

    Caplin Point Laboratories Limited

    India
    Nutri Ingredients Summit
    Not Confirmed
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    Caplin Point Laboratories Limited

    India
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 1.34GM/5ML;1.38GM/5ML (268MG/ML; 276MG/ML)

    Packaging :

    Approval Date : 2026-02-23

    Application Number : 220683

    Regulatory Info : RX

    Registration Country : USA

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    11

    Caplin Point Laboratories Limited

    India
    Nutri Ingredients Summit
    Not Confirmed
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    Caplin Point Laboratories Limited

    India
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML; 276MG/ML)

    Packaging :

    Approval Date : 2026-02-23

    Application Number : 220683

    Regulatory Info : RX

    Registration Country : USA

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    12

    Caplin Point Laboratories Limited

    India
    Nutri Ingredients Summit
    Not Confirmed
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    Caplin Point Laboratories Limited

    India
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 13.4GM/50ML;13.8GM/50ML (268MG/ML; 276MG/ML)

    Packaging :

    Approval Date : 2026-02-23

    Application Number : 220683

    Regulatory Info : RX

    Registration Country : USA

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    13

    Fresenius Kabi USA

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Nutri Ingredients Summit
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2022-03-30

    Application Number : 209997

    Regulatory Info : RX

    Registration Country : USA

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    14

    Fresenius Kabi USA

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2022-03-30

    Application Number : 209997

    Regulatory Info : RX

    Registration Country : USA

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    15

    Fresenius Kabi USA

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 2022-03-30

    Application Number : 209997

    Regulatory Info : RX

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

    Brand Name : SODIUM PHOSPHATES IN PLASTIC CONTAINER

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)

    Packaging :

    Approval Date : 1983-05-10

    Application Number : 18892

    Regulatory Info : RX

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Packaging :

    Approval Date : 1988-11-01

    Application Number : 19682

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Hospira, Inc.

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4.25%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

    Packaging :

    Approval Date : 1988-11-01

    Application Number : 19682

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    ICU Medical

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    ICU Medical

    U.S.A
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    Nutri Ingredients Summit
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : AMINOSYN II 3.5% M

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 3.5%;30MG/100ML;97MG/100ML;120MG/100ML;49MG/100ML

    Packaging :

    Approval Date : 1986-04-03

    Application Number : 19437

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Lukare medical

    U.S.A
    Nutri Ingredients Summit
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    Lukare medical

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    Nutri Ingredients Summit
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    Regulatory Info : RX

    Registration Country : USA

    CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : ELLIOTTS B SOLUTION

    Dosage Form : INJECTABLE;INTRATHECAL

    Dosage Strength : 0.2MG/ML;0.8MG/ML;0.3MG/ML;0.3MG/ML;1.9MG/ML;7.3MG/ML;0.2MG/ML

    Packaging :

    Approval Date : 1996-09-27

    Application Number : 20577

    Regulatory Info : RX

    Registration Country : USA

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