Search by Drug Name or NDC

    NDC 70518-0451-03 Allopurinol 100 mg/1 Details

    Allopurinol 100 mg/1

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

    Product Information

    NDC 70518-0451
    Product ID 70518-0451_0e36beb1-f027-8687-e063-6294a90aef25
    Associated GPIs 68000010000305
    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 Allopurinol
    Proprietary Name Suffix n/a
    Non-Proprietary Name allopurinol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name ALLOPURINOL
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203154
    Listing Certified Through 2025-12-31

    Package

    NDC 70518-0451-03 (70518045103)

    NDC Package Code 70518-0451-3
    Billing NDC 70518045103
    Package 180 TABLET in 1 BOTTLE, PLASTIC (70518-0451-3)
    Marketing Start Date 2021-11-12
    NDC Exclude Flag N
    Pricing Information N/A