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    NDC 59746-0324-10 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 Jubilant Cadista Pharmaceuticals Inc.. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 59746-0324
    Product ID 59746-324_40211dd2-c21e-45a4-a8d4-04febf925f52
    Associated GPIs 12405085100310
    GCN Sequence Number 023989
    GCN Sequence Number Description valacyclovir HCl TABLET 500 MG ORAL
    HIC3 W5A
    HIC3 Description ANTIVIRALS, GENERAL
    GCN 13740
    HICL Sequence Number 010117
    HICL Sequence Number Description VALACYCLOVIR HCL
    Brand/Generic Generic
    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 Jubilant Cadista 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 ANDA201506
    Listing Certified Through 2024-12-31

    Package

    NDC 59746-0324-10 (59746032410)

    NDC Package Code 59746-324-10
    Billing NDC 59746032410
    Package 10 TABLET, FILM COATED in 1 BOTTLE (59746-324-10)
    Marketing Start Date 2012-04-05
    NDC Exclude Flag N
    Pricing Information N/A