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    Acrotech Biopharma

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    LEVOLEUCOVORIN CALCIUM

    Brand Name : FUSILEV

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    Dosage Strength : EQ 50MG BASE/VIAL

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    Approval Date : 2008-03-07

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    Acrotech Biopharma

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    Brand Name : FUSILEV

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    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2011-04-29

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    LEVOLEUCOVORIN CALCIUM

    Brand Name : FUSILEV

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    LEVOLEUCOVORIN CALCIUM

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    Approval Date : 2017-02-13

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    LEVOLEUCOVORIN CALCIUM

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    Approval Date : 2016-09-29

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    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    GLAND PHARMA LIMITED

    India
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    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2018-09-14

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    LEVOLEUCOVORIN CALCIUM

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    Dosage Strength : EQ 250MG BASE/25ML (EQ 10MG BASE/ML)

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    Hikma Pharmaceuticals

    United Kingdom
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    Dosage Strength : EQ 50MG BASE/VIAL

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    Approval Date : 2016-06-16

    Application Number : 206263

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    Meitheal Pharmaceuticals

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    LEVOLEUCOVORIN CALCIUM

    Brand Name : LEVOLEUCOVORIN CALCIUM

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2019-08-16

    Application Number : 211002

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    Meitheal Pharmaceuticals

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    LEVOLEUCOVORIN CALCIUM

    Brand Name : LEVOLEUCOVORIN CALCIUM

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 250MG BASE/25ML (EQ 10MG BASE/ML)

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    Approval Date : 2019-08-16

    Application Number : 211002

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    Meitheal Pharmaceuticals

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    LEVOLEUCOVORIN CALCIUM

    Brand Name : LEVOLEUCOVORIN CALCIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

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    Approval Date : 2019-08-22

    Application Number : 211003

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    Norvium

    U.S.A
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    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2015-10-20

    Application Number : 203576

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    Norvium

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    Dosage Strength : EQ 250MG BASE/25ML (EQ 10MG BASE/ML)

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    Approval Date : 2015-10-20

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    Novast Laboratories

    China
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    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2018-05-03

    Application Number : 210623

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    Novast Laboratories

    China
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    Praxgen

    U.S.A
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    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2021-11-02

    Application Number : 213797

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    Sandoz B2B

    Switzerland
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    Dosage Strength : EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)

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    Approval Date : 2015-03-09

    Application Number : 203563

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    Sandoz B2B

    Switzerland
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    Dosage Strength : EQ 250MG BASE/25ML (EQ 10MG BASE/ML)

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    Approval Date : 2015-03-09

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