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    NDC 53002-0640-02 Famciclovir 250 mg/1 Details

    Famciclovir 250 mg/1

    Famciclovir is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is FAMCICLOVIR.

    Product Information

    NDC 53002-0640
    Product ID 53002-0640_07873151-03d7-4426-bc48-57537620b2b4
    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 Famciclovir
    Proprietary Name Suffix n/a
    Non-Proprietary Name Famciclovir
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name FAMCICLOVIR
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class DNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202438
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-0640-02 (53002064002)

    NDC Package Code 53002-0640-2
    Billing NDC 53002064002
    Package 20 TABLET, FILM COATED in 1 BOTTLE (53002-0640-2)
    Marketing Start Date 2022-01-01
    NDC Exclude Flag N
    Pricing Information N/A