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    NDC 68788-7063-01 aripiprazole 20 mg/1 Details

    aripiprazole 20 mg/1

    aripiprazole is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is ARIPIPRAZOLE.

    Product Information

    NDC 68788-7063
    Product ID 68788-7063_2068c32e-ef07-45e5-b6c6-b1fb68f28a50
    Associated GPIs 59250015000340
    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 aripiprazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name aripiprazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ARIPIPRAZOLE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Atypical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201519
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7063-01 (68788706301)

    NDC Package Code 68788-7063-1
    Billing NDC 68788706301
    Package 100 TABLET in 1 BOTTLE (68788-7063-1)
    Marketing Start Date 2018-01-05
    NDC Exclude Flag N
    Pricing Information N/A