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    NDC 35356-0733-20 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 Quality Care Products, LLC. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 35356-0733
    Product ID 35356-733_f669a7c7-742e-4ef5-9ef4-d2c91bd239d7
    Associated GPIs 05000020100315
    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
    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 Quality Care Products, LLC
    Pharmaceutical Class Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075593
    Listing Certified Through 2024-12-31

    Package

    NDC 35356-0733-20 (35356073320)

    NDC Package Code 35356-733-20
    Billing NDC 35356073320
    Package 20 TABLET, FILM COATED in 1 BOTTLE (35356-733-20)
    Marketing Start Date 2019-05-24
    NDC Exclude Flag N
    Pricing Information N/A