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    NDC 61919-0748-90 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 DIRECT RX. The primary component is ALLOPURINOL.

    Product Information

    NDC 61919-0748
    Product ID 61919-748_b932a9e5-7d66-0bf1-e053-2995a90a4414
    Associated GPIs 68000010000305
    GCN Sequence Number 002535
    GCN Sequence Number Description allopurinol TABLET 100 MG ORAL
    HIC3 C7A
    HIC3 Description HYPERURICEMIA TX - XANTHINE OXIDASE INHIBITORS
    GCN 07070
    HICL Sequence Number 001100
    HICL Sequence Number Description ALLOPURINOL
    Brand/Generic Generic
    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 DIRECT RX
    Pharmaceutical Class Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203154
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0748-90 (61919074890)

    NDC Package Code 61919-748-90
    Billing NDC 61919074890
    Package 90 TABLET in 1 BOTTLE (61919-748-90)
    Marketing Start Date 2021-01-18
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 67604124-399e-7baf-e053-2a91aa0a8ee8 Details

    Revised: 1/2021