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    NDC 00338-0720-01 PEMETREXED 100 mg/10mL Details

    PEMETREXED 100 mg/10mL

    PEMETREXED is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is PEMETREXED DISODIUM HEPTAHYDRATE.

    Product Information

    NDC 00338-0720
    Product ID 0338-0720_49e02e19-8abb-4fa7-a69c-6df8bdb102f6
    Associated GPIs
    GCN Sequence Number 063546
    GCN Sequence Number Description pemetrexed disodium VIAL 100 MG INTRAVEN
    HIC3 V1B
    HIC3 Description ANTINEOPLASTIC - ANTIMETABOLITES
    GCN 99268
    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
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 100
    Active Ingredient Units mg/10mL
    Substance Name PEMETREXED DISODIUM HEPTAHYDRATE
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214436
    Listing Certified Through 2024-12-31

    Package

    NDC 00338-0720-01 (00338072001)

    NDC Package Code 0338-0720-01
    Billing NDC 00338072001
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0338-0720-01) / 10 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2022-08-18
    NDC Exclude Flag N
    Pricing Information N/A