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    NDC 70518-3263-03 Methotrexate 2.5 mg/1 Details

    Methotrexate 2.5 mg/1

    Methotrexate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is METHOTREXATE SODIUM.

    Product Information

    NDC 70518-3263
    Product ID 70518-3263_06bc5947-7cbe-3b4f-e063-6394a90ae327
    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 Methotrexate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methotrexate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name METHOTREXATE SODIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213343
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3263-03 (70518326303)

    NDC Package Code 70518-3263-3
    Billing NDC 70518326303
    Package 12 TABLET in 1 BOTTLE, PLASTIC (70518-3263-3)
    Marketing Start Date 2022-09-11
    NDC Exclude Flag N
    Pricing Information N/A