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    NDC 53002-0271-00 Acyclovir 800 mg/1 Details

    Acyclovir 800 mg/1

    Acyclovir is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is ACYCLOVIR.

    Product Information

    NDC 53002-0271
    Product ID 53002-0271_fdc34522-21a2-426f-9f04-1ffd8a4f0c4b
    Associated GPIs 04000020100310
    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 Acyclovir
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acyclovir
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 800
    Active Ingredient Units mg/1
    Substance Name ACYCLOVIR
    Labeler Name RPK 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 ANDA075382
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-0271-00 (53002027100)

    NDC Package Code 53002-0271-0
    Billing NDC 53002027100
    Package 50 TABLET in 1 BOTTLE (53002-0271-0)
    Marketing Start Date 2020-01-01
    NDC Exclude Flag N
    Pricing Information N/A