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    NDC 71335-0123-07 Valacyclovir hydrochloride 1000 mg/1 Details

    Valacyclovir hydrochloride 1000 mg/1

    Valacyclovir hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 71335-0123
    Product ID 71335-0123_f16a9466-f381-40ba-aa6f-36854837af01
    Associated GPIs 12405085100320
    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 1000
    Active Ingredient Units mg/1
    Substance Name VALACYCLOVIR HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    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 2023-12-31

    Package

    NDC 71335-0123-07 (71335012307)

    NDC Package Code 71335-0123-7
    Billing NDC 71335012307
    Package 15 TABLET in 1 BOTTLE (71335-0123-7)
    Marketing Start Date 2022-02-23
    NDC Exclude Flag N
    Pricing Information N/A