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    NDC 70518-1278-00 Ciprofloxacin 500 mg/1 Details

    Ciprofloxacin 500 mg/1

    Ciprofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 70518-1278
    Product ID 70518-1278_0877d649-1dcd-e2c4-e063-6294a90ac907
    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 Ciprofloxacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ciprofloxacin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077859
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1278-00 (70518127800)

    NDC Package Code 70518-1278-0
    Billing NDC 70518127800
    Package 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1278-0)
    Marketing Start Date 2018-06-26
    NDC Exclude Flag N
    Pricing Information N/A