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    NDC 71335-1862-09 Valacyclovir Hydrochloride 1 g/1 Details

    Valacyclovir Hydrochloride 1 g/1

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

    Product Information

    NDC 71335-1862
    Product ID 71335-1862_9ea87f54-eb20-4baf-bbd1-d346e1102093
    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 1
    Active Ingredient Units g/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 ANDA090682
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1862-09 (71335186209)

    NDC Package Code 71335-1862-9
    Billing NDC 71335186209
    Package 90 TABLET, FILM COATED in 1 BOTTLE (71335-1862-9)
    Marketing Start Date 2021-10-21
    NDC Exclude Flag N
    Pricing Information N/A