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    NDC 55154-7985-00 Valacyclovir Hydrochloride 500 mg/1 Details

    Valacyclovir Hydrochloride 500 mg/1

    Valacyclovir Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 55154-7985
    Product ID 55154-7985_389af6c8-387a-4ce2-9eee-4ab434c1108a
    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 Valacyclovir Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Valacyclovir Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name VALACYCLOVIR HYDROCHLORIDE
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090682
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-7985-00 (55154798500)

    NDC Package Code 55154-7985-0
    Billing NDC 55154798500
    Package 10 BLISTER PACK in 1 BAG (55154-7985-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2010-05-24
    NDC Exclude Flag N
    Pricing Information N/A