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    NDC 50090-3537-00 donepezil hydrochloride 5 mg/1 Details

    donepezil hydrochloride 5 mg/1

    donepezil hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is DONEPEZIL HYDROCHLORIDE.

    Product Information

    NDC 50090-3537
    Product ID 50090-3537_88e8acb5-251c-442e-bd88-ea7cd0416c6e
    Associated GPIs 62051025100310
    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 5
    Active Ingredient Units mg/1
    Substance Name DONEPEZIL HYDROCHLORIDE
    Labeler Name A-S Medication Solutions
    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 50090-3537-00 (50090353700)

    NDC Package Code 50090-3537-0
    Billing NDC 50090353700
    Package 90 TABLET, FILM COATED in 1 BOTTLE (50090-3537-0)
    Marketing Start Date 2018-08-15
    NDC Exclude Flag N
    Pricing Information N/A