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    NDC 68788-8203-08 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 Preferred Pharmaceuticals Inc.. The primary component is ACYCLOVIR.

    Product Information

    NDC 68788-8203
    Product ID 68788-8203_ea6fb7a8-80b1-4a00-af54-e55ca13084a2
    Associated GPIs 12405010000320
    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 400
    Active Ingredient Units mg/1
    Substance Name ACYCLOVIR
    Labeler Name Preferred 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 ANDA209366
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8203-08 (68788820308)

    NDC Package Code 68788-8203-8
    Billing NDC 68788820308
    Package 35 TABLET in 1 BOTTLE (68788-8203-8)
    Marketing Start Date 2022-05-26
    NDC Exclude Flag N
    Pricing Information N/A