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    NDC 51672-4184-04 Iloperidone 12 mg/1 Details

    Iloperidone 12 mg/1

    Iloperidone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is ILOPERIDONE.

    Product Information

    NDC 51672-4184
    Product ID 51672-4184_6787555e-8a11-481c-b05c-179b0aedcf5c
    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 Iloperidone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Iloperidone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 12
    Active Ingredient Units mg/1
    Substance Name ILOPERIDONE
    Labeler Name Taro Pharmaceuticals U.S.A., Inc.
    Pharmaceutical Class Atypical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207098
    Listing Certified Through 2024-12-31

    Package

    NDC 51672-4184-04 (51672418404)

    NDC Package Code 51672-4184-4
    Billing NDC 51672418404
    Package 60 TABLET in 1 BOTTLE (51672-4184-4)
    Marketing Start Date 2019-07-22
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6f17cc91-86b3-42e3-9bf2-935dd360c3eb Details

    Revised: 8/2019