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    Dr. Reddy's Laboratories

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    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

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    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2022-05-25

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    Dr. Reddy's Laboratories

    India
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    PEMETREXED DISODIUM

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    Dosage Strength : EQ 500MG BASE/VIAL

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    03

    Dr. Reddy's Laboratories

    India
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    PEMETREXED DISODIUM

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    Dosage Strength : EQ 1GM BASE/VIAL

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    Application Number : 202596

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    04

    Accord healthcare

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    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 203485

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    05

    Accord healthcare

    United Kingdom
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    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 203485

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    06

    Accord healthcare

    United Kingdom
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    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 203485

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    07

    Apotex Inc

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    Approval Date : 2022-05-25

    Application Number : 203774

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    Approval Date : 2022-05-25

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    09

    Eli Lilly

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    PEMETREXED DISODIUM

    Brand Name : ALIMTA

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2004-02-04

    Application Number : 21462

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    10

    Eli Lilly

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    Brand Name : ALIMTA

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2007-09-07

    Application Number : 21462

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    11

    Fresenius Kabi USA

    U.S.A
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    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 90384

    Regulatory Info : RX

    Registration Country : USA

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    12

    Fresenius Kabi USA

    U.S.A
    Simposio AFI
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Simposio AFI
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    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 90384

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    Registration Country : USA

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    13

    Fresenius Kabi USA

    U.S.A
    Simposio AFI
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Simposio AFI
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    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 750MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 90384

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    Registration Country : USA

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    14

    Fresenius Kabi USA

    U.S.A
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    Fresenius Kabi USA

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    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 90384

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    15

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 202111

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    Simposio AFI
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    Hospira, Inc.

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    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 202111

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 202111

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Norvium

    U.S.A
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    Norvium

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2023-03-10

    Application Number : 203628

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Qilu Pharmaceutical

    China
    Simposio AFI
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    Qilu Pharmaceutical

    China
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    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

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    Approval Date : 2022-05-25

    Application Number : 204890

    Regulatory Info : RX

    Registration Country : USA

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    20

    Teva Pharmaceutical Industries

    Israel
    Simposio AFI
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Simposio AFI
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    PEMETREXED SODIUM

    Brand Name : PEMETREXED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG

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    Approval Date :

    Application Number : 90352

    Regulatory Info :

    Registration Country : USA

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