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    NDC 68382-0154-06 risperidone 0.5 mg/1 Details

    risperidone 0.5 mg/1

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

    Product Information

    NDC 68382-0154
    Product ID 68382-154_039dfd45-2fd7-4938-a2a7-3959fa4e1ee6
    Associated GPIs
    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 risperidone
    Proprietary Name Suffix n/a
    Non-Proprietary Name risperidone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, ORALLY DISINTEGRATING
    Route ORAL
    Active Ingredient Strength 0.5
    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 ANDA078516
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0154-06 (68382015406)

    NDC Package Code 68382-154-06
    Billing NDC 68382015406
    Package 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-154-06)
    Marketing Start Date 2010-06-29
    NDC Exclude Flag N
    Pricing Information N/A