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    NDC 70934-0628-21 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is VALACYCLOVIR HYDROCHLORIDE.

    Product Information

    NDC 70934-0628
    Product ID 70934-628_e60fa049-cada-65c6-e053-2995a90a4481
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0628-21 (70934062821)

    NDC Package Code 70934-628-21
    Billing NDC 70934062821
    Package 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-628-21)
    Marketing Start Date 2022-08-05
    NDC Exclude Flag N
    Pricing Information N/A
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