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    01 3DR REDDYS LABS INC

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    01

    DR REDDYS LABS INC

    India
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    CPhI India 2024
    Booth #RH.E02
    • 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 :

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED FOR INJECTION

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100MG

    Approval Date :

    Application Number : 208297

    RX/OTC/DISCN :

    RLD :

    TE Code :

    Dr Reddy Company Banner

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    02

    DR REDDYS LABS INC

    India
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    CPhI India 2024
    Booth #RH.E02
    • 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 :

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED FOR INJECTION

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG

    Approval Date :

    Application Number : 208297

    RX/OTC/DISCN :

    RLD :

    TE Code :

    Dr Reddy Company Banner

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    03

    DR REDDYS LABS INC

    India
    arrow
    CPhI India 2024
    Booth #RH.E02
    • fda
    • EDQM
    • WHO-GMP

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

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    Flag India
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    RLD :

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED FOR INJECTION

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1G

    Approval Date :

    Application Number : 208297

    RX/OTC/DISCN :

    RLD :

    TE Code :

    Dr Reddy Company Banner

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    04

    ACTAVIS

    Ireland
    Pharmtech & Ingredients
    Not Confirmed
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    ACTAVIS

    Ireland
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    Pharmtech & Ingredients
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    • fda
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    RLD : Yes

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 100MG/4ML (25MG/ML)

    Approval Date : 2020-08-21

    Application Number : 208419

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    05

    ACTAVIS

    Ireland
    Pharmtech & Ingredients
    Not Confirmed
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    ACTAVIS

    Ireland
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 500MG/20ML (25MG/ML)

    Approval Date : 2020-08-21

    Application Number : 208419

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

    Portfolio PDF

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    06

    ACTAVIS

    Ireland
    Pharmtech & Ingredients
    Not Confirmed
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    ACTAVIS

    Ireland
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag Ireland
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    RLD : Yes

    TE Code :

    PEMETREXED

    Brand Name : PEMETREXED

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 1GM/40ML (25MG/ML)

    Approval Date : 2020-08-21

    Application Number : 208419

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

    Portfolio PDF

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    Virtual Booth

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    07

    BIOCON LTD

    India
    Pharmtech & Ingredients
    Not Confirmed
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    08

    BIOCON LTD

    India
    Pharmtech & Ingredients
    Not Confirmed
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    09

    EAGLE PHARMS

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    EAGLE PHARMS

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    PEMETREXED

    Brand Name : PEMFEXY

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 500MG/20ML (25MG/ML)

    Approval Date : 2020-02-08

    Application Number : 209472

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    10

    LILLY

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    LILLY

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD :

    TE Code :

    PEMETREXED

    Brand Name : ALIMTA

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 500MG

    Approval Date :

    Application Number : 21677

    RX/OTC/DISCN :

    RLD :

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF