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    NDC 71205-0243-90 ACYCLOVIR 200 mg/1 Details

    ACYCLOVIR 200 mg/1

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

    Product Information

    NDC 71205-0243
    Product ID 71205-243_c225060d-b6e8-4343-8e4d-b52067f05792
    Associated GPIs 12405010000110
    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 CAPSULE
    Route ORAL
    Active Ingredient Strength 200
    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 ANDA075677
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0243-90 (71205024390)

    NDC Package Code 71205-243-90
    Billing NDC 71205024390
    Package 90 CAPSULE in 1 BOTTLE (71205-243-90)
    Marketing Start Date 2019-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 8d7994a6-5bd2-494d-89c1-b03755d4f2c3 Details

    Revised: 12/2020