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    NDC 72338-0100-01 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 Waverley Pharma Inc. The primary component is PEMETREXED DISODIUM HEPTAHYDRATE.

    Product Information

    NDC 72338-0100
    Product ID 72338-100_d0687ba7-a598-4409-8459-0204bcb6d9f3
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 HEPTAHYDRATE
    Labeler Name Waverley Pharma Inc
    Pharmaceutical Class Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211899
    Listing Certified Through 2025-12-31

    Package

    NDC 72338-0100-01 (72338010001)

    NDC Package Code 72338-100-01
    Billing NDC 72338010001
    Package 1 VIAL in 1 CARTON (72338-100-01) / 4 mL in 1 VIAL
    Marketing Start Date 2018-06-04
    NDC Exclude Flag N
    Pricing Information N/A