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    NDC 68071-1523-03 donepezil hydrochloride 10 mg/1 Details

    donepezil hydrochloride 10 mg/1

    donepezil hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by NuCare Pharmaceuticals,Inc.. The primary component is DONEPEZIL HYDROCHLORIDE.

    Product Information

    NDC 68071-1523
    Product ID 68071-1523_d5d067d8-3e69-66a9-e053-2995a90a6ece
    Associated GPIs 62051025100320
    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 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 10
    Active Ingredient Units mg/1
    Substance Name DONEPEZIL HYDROCHLORIDE
    Labeler Name NuCare Pharmaceuticals,Inc.
    Pharmaceutical Class Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA200292
    Listing Certified Through 2024-12-31

    Package

    NDC 68071-1523-03 (68071152303)

    NDC Package Code 68071-1523-3
    Billing NDC 68071152303
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68071-1523-3)
    Marketing Start Date 2017-07-18
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 549e48a5-be62-0042-e054-00144ff8d46c Details

    Revised: 1/2022