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    NDC 63629-8483-01 Donepezil Hydrochloride 23 mg/1 Details

    Donepezil Hydrochloride 23 mg/1

    Donepezil Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is DONEPEZIL HYDROCHLORIDE.

    Product Information

    NDC 63629-8483
    Product ID 63629-8483_6f78fe1c-7057-41ef-bea2-4f932a842178
    Associated GPIs 62051025100330
    GCN Sequence Number 066533
    GCN Sequence Number Description donepezil HCl TABLET 23 MG ORAL
    HIC3 J1B
    HIC3 Description CHOLINESTERASE INHIBITORS
    GCN 28828
    HICL Sequence Number 012259
    HICL Sequence Number Description DONEPEZIL HCL
    Brand/Generic Generic
    Proprietary Name Donepezil Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Donepezil Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 23
    Active Ingredient Units mg/1
    Substance Name DONEPEZIL HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203104
    Listing Certified Through 2025-12-31

    Package

    NDC 63629-8483-01 (63629848301)

    NDC Package Code 63629-8483-1
    Billing NDC 63629848301
    Package 30 TABLET, FILM COATED in 1 BOTTLE (63629-8483-1)
    Marketing Start Date 2021-05-18
    NDC Exclude Flag N
    Pricing Information N/A