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    NDC 71205-0056-30 Acyclovir 400 mg/1 Details

    Acyclovir 400 mg/1

    Acyclovir is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is ACYCLOVIR.

    Product Information

    NDC 71205-0056
    Product ID 71205-056_7fadb9ce-34cc-4b19-9470-15e3a64d9c4f
    Associated GPIs 12405010000320
    GCN Sequence Number 016408
    GCN Sequence Number Description acyclovir TABLET 400 MG ORAL
    HIC3 W5A
    HIC3 Description ANTIVIRALS, GENERAL
    GCN 13724
    HICL Sequence Number 004183
    HICL Sequence Number Description ACYCLOVIR
    Brand/Generic Generic
    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 400
    Active Ingredient Units mg/1
    Substance Name ACYCLOVIR
    Labeler Name Proficient Rx LP
    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 71205-0056-30 (71205005630)

    NDC Package Code 71205-056-30
    Billing NDC 71205005630
    Package 30 TABLET in 1 BOTTLE, PLASTIC (71205-056-30)
    Marketing Start Date 2018-06-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 33630a35-346e-43b6-9286-89e28ac0094a Details

    Revised: 6/2022