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    NDC 42708-0002-14 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 QPharma Inc. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 42708-0002
    Product ID 42708-002_f2682ce3-8cfd-df80-e053-2a95a90ac08a
    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
    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 QPharma Inc
    Pharmaceutical Class Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076794
    Listing Certified Through 2024-12-31

    Package

    NDC 42708-0002-14 (42708000214)

    NDC Package Code 42708-002-14
    Billing NDC 42708000214
    Package 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-002-14)
    Marketing Start Date 2018-05-09
    NDC Exclude Flag N
    Pricing Information N/A