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    NDC 50090-1735-02 Valacyclovir hydrochloride 500 mg/1 Details

    Valacyclovir hydrochloride 500 mg/1

    Valacyclovir hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 50090-1735
    Product ID 50090-1735_8f7abb2d-978d-4f26-b2be-de49d329963a
    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
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name VALACYCLOVIR HYDROCHLORIDE
    Labeler Name A-S Medication Solutions
    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 ANDA077135
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-1735-02 (50090173502)

    NDC Package Code 50090-1735-2
    Billing NDC 50090173502
    Package 30 TABLET in 1 BOTTLE (50090-1735-2)
    Marketing Start Date 2015-03-10
    NDC Exclude Flag N
    Pricing Information N/A