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    NDC 66267-0665-30 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 NuCare Pharmaceuticals, Inc.. The primary component is ALLOPURINOL.

    Product Information

    NDC 66267-0665
    Product ID 66267-665_e3169e46-0210-680e-e053-2a95a90abe5e
    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 NuCare Pharmaceuticals, Inc.
    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 66267-0665-30 (66267066530)

    NDC Package Code 66267-665-30
    Billing NDC 66267066530
    Package 30 TABLET in 1 BOTTLE (66267-665-30)
    Marketing Start Date 2016-12-28
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 44bcc8df-a803-010f-e054-00144ff88e88 Details

    Revised: 7/2022