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    NDC 50742-0341-01 Pemetrexed 500 mg/20mL Details

    Pemetrexed 500 mg/20mL

    Pemetrexed is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ingenus Pharmaceuticals, LLC. The primary component is PEMETREXED DISODIUM HEMIPENTAHYDRATE.

    Product Information

    NDC 50742-0341
    Product ID 50742-341_e370870e-837c-4405-82a4-95f5c8824217
    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 Generic
    Proprietary Name Pemetrexed
    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 HEMIPENTAHYDRATE
    Labeler Name Ingenus Pharmaceuticals, LLC
    Pharmaceutical Class Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204890
    Listing Certified Through 2024-12-31

    Package

    NDC 50742-0341-01 (50742034101)

    NDC Package Code 50742-341-01
    Billing NDC 50742034101
    Package 1 VIAL in 1 CARTON (50742-341-01) / 20 mL in 1 VIAL
    Marketing Start Date 2022-05-24
    NDC Exclude Flag N
    Pricing Information N/A