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    Approved Drug Products containing Pemetrexed Disodium Hemipentahydrate listed in the FDA Orange Book. Original Data : FDA Website

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Pemetrexed Disodium Hemipentahydrate

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 3DR REDDYS

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    17 2QILU PHARM HAINAN

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    01

    DR REDDYS

    India
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    CPhI Worldwide, Milan
    Booth #24A41
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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 202596

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    DR REDDYS

    India
    arrow
    CPhI Worldwide, Milan
    Booth #24A41
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 202596

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    DR REDDYS

    India
    arrow
    CPhI Worldwide, Milan
    Booth #24A41
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 202596

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

    Dr Reddy Company Banner

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    04

    LILLY

    U.S.A
    Discovery on Target
    Not Confirmed
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    LILLY

    U.S.A
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    RLD : Yes

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : ALIMTA

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 2004-02-04

    Application Number : 21462

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    05

    LILLY

    U.S.A
    Discovery on Target
    Not Confirmed
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    LILLY

    U.S.A
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    Discovery on Target
    Not Confirmed
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    RLD : Yes

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : ALIMTA

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2007-09-07

    Application Number : 21462

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    06

    FRESENIUS KABI USA

    U.S.A
    Discovery on Target
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 90384

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    FRESENIUS KABI USA

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    FRESENIUS KABI USA

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 90384

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    FRESENIUS KABI USA

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    FRESENIUS KABI USA

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 750MG BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 90384

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    09

    FRESENIUS KABI USA

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    FRESENIUS KABI USA

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    PEMETREXED DISODIUM

    Brand Name : PEMETREXED DISODIUM

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 2022-05-25

    Application Number : 90384

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    TEVA PHARMS USA

    Israel
    Discovery on Target
    Not Confirmed
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    TEVA PHARMS USA

    Israel
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    Discovery on Target
    Not Confirmed
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    RLD :

    TE Code :

    PEMETREXED SODIUM

    Brand Name : PEMETREXED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG

    Approval Date :

    Application Number : 90352

    RX/OTC/DISCN :

    RLD :

    TE Code :

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