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    NDC 68001-0538-41 Pemetrexed 100 mg/4mL Details

    Pemetrexed 100 mg/4mL

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

    Product Information

    NDC 68001-0538
    Product ID 68001-538_eed98f1e-acdf-28da-e053-2a95a90a046c
    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 disodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 100
    Active Ingredient Units mg/4mL
    Substance Name PEMETREXED DISODIUM HEMIPENTAHYDRATE
    Labeler Name BluePoint Laboratories
    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 68001-0538-41 (68001053841)

    NDC Package Code 68001-538-41
    Billing NDC 68001053841
    Package 1 VIAL in 1 CARTON (68001-538-41) / 4 mL in 1 VIAL
    Marketing Start Date 2022-06-24
    NDC Exclude Flag N
    Pricing Information N/A