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    NDC 00002-7623-01 Alimta 500 mg/20mL Details

    Alimta 500 mg/20mL

    Alimta is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eli Lilly and Company. The primary component is PEMETREXED DISODIUM HEPTAHYDRATE.

    Product Information

    NDC 00002-7623
    Product ID 0002-7623_3af0bc84-13d6-46aa-a4c0-c62410b73bc6
    Associated GPIs 21300053102120
    GCN Sequence Number 053600
    GCN Sequence Number Description pemetrexed disodium VIAL 500 MG INTRAVEN
    HIC3 V1B
    HIC3 Description ANTINEOPLASTIC - ANTIMETABOLITES
    GCN 21179
    HICL Sequence Number 025905
    HICL Sequence Number Description PEMETREXED DISODIUM
    Brand/Generic Brand
    Proprietary Name Alimta
    Proprietary Name Suffix n/a
    Non-Proprietary Name Pemetrexed disodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 500
    Active Ingredient Units mg/20mL
    Substance Name PEMETREXED DISODIUM HEPTAHYDRATE
    Labeler Name Eli Lilly and Company
    Pharmaceutical Class Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021462
    Listing Certified Through 2024-12-31

    Package

    NDC 00002-7623-01 (00002762301)

    NDC Package Code 0002-7623-01
    Billing NDC 00002762301
    Package 1 VIAL in 1 CARTON (0002-7623-01) / 20 mL in 1 VIAL
    Marketing Start Date 2004-02-13
    NDC Exclude Flag N
    Pricing Information N/A