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    NDC 68788-6896-07 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 Preferred Pharmaceuticals Inc.. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 68788-6896
    Product ID 68788-6896_8fa04a03-72ac-40fa-a3d9-423cfd9fa7d0
    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 Preferred Pharmaceuticals Inc.
    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 68788-6896-07 (68788689607)

    NDC Package Code 68788-6896-7
    Billing NDC 68788689607
    Package 21 TABLET in 1 BOTTLE (68788-6896-7)
    Marketing Start Date 2017-02-13
    NDC Exclude Flag N
    Pricing Information N/A