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    NDC 69292-0580-01 Haloperidol 0.5 mg/1 Details

    Haloperidol 0.5 mg/1

    Haloperidol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amici Pharmaceuticals, LLC. The primary component is HALOPERIDOL.

    Product Information

    NDC 69292-0580
    Product ID 69292-580_8c9cdd3d-9751-404a-9ceb-276e8dfa6391
    Associated GPIs 59100010100305
    GCN Sequence Number 003972
    GCN Sequence Number Description haloperidol TABLET 0.5 MG ORAL
    HIC3 H7O
    HIC3 Description ANTIPSYCHOTICS,DOPAMINE ANTAGONISTS,BUTYROPHENONES
    GCN 15530
    HICL Sequence Number 001662
    HICL Sequence Number Description HALOPERIDOL
    Brand/Generic Generic
    Proprietary Name Haloperidol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Haloperidol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name HALOPERIDOL
    Labeler Name Amici Pharmaceuticals, LLC
    Pharmaceutical Class Typical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA071173
    Listing Certified Through 2024-12-31

    Package

    NDC 69292-0580-01 (69292058001)

    NDC Package Code 69292-580-01
    Billing NDC 69292058001
    Package 100 TABLET in 1 BOTTLE (69292-580-01)
    Marketing Start Date 2022-04-18
    NDC Exclude Flag N
    Pricing Information
    Price Per Unit 0.24362
    Pricing Unit EA
    Effective Date 2022-11-23
    NDC Description HALOPERIDOL 0.5 MG TABLET
    Pharmacy Type Indicator C/I
    OTC N
    Explanation Code 1
    Classification for Rate Setting G
    As of Date 2022-11-23
    This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

    Standard Product Labeling (SPL)/Prescribing Information SPL 9a9e20dd-646a-4fe9-a345-1b5bda8e7775 Details

    Revised: 5/2022