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    NDC 70518-1398-03 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.

    Product Information

    NDC 70518-1398
    Product ID 70518-1398_0a49a8eb-1829-a142-e063-6394a90ad3f7
    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
    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 ANDA207812
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1398-03 (70518139803)

    NDC Package Code 70518-1398-3
    Billing NDC 70518139803
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70518-1398-3)
    Marketing Start Date 2018-11-15
    NDC Exclude Flag N
    Pricing Information N/A