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    NDC 68382-0114-01 risperidone 1 mg/1 Details

    risperidone 1 mg/1

    risperidone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is RISPERIDONE.

    Product Information

    NDC 68382-0114
    Product ID 68382-114_fc6e6540-fc7f-4329-b05b-5ec4ffd57000
    Associated GPIs 59070070000310
    GCN Sequence Number 021154
    GCN Sequence Number Description risperidone TABLET 1 MG ORAL
    HIC3 H7T
    HIC3 Description ANTIPSYCHOTIC,ATYPICAL,DOPAMINE,SEROTONIN ANTAGNST
    GCN 16136
    HICL Sequence Number 008721
    HICL Sequence Number Description RISPERIDONE
    Brand/Generic Generic
    Proprietary Name risperidone
    Proprietary Name Suffix n/a
    Non-Proprietary Name risperidone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name RISPERIDONE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Atypical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078040
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0114-01 (68382011401)

    NDC Package Code 68382-114-01
    Billing NDC 68382011401
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68382-114-01)
    Marketing Start Date 2008-11-13
    NDC Exclude Flag N
    Pricing Information N/A