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    NDC 50090-2146-01 Ciprofloxacin 250 mg/1 Details

    Ciprofloxacin 250 mg/1

    Ciprofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 50090-2146
    Product ID 50090-2146_39dc1282-e407-4a13-bf0c-21af9463db10
    Associated GPIs 05000020100310
    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 250
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name A-S Medication Solutions
    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 50090-2146-01 (50090214601)

    NDC Package Code 50090-2146-1
    Billing NDC 50090214601
    Package 14 TABLET, FILM COATED in 1 BOTTLE (50090-2146-1)
    Marketing Start Date 2015-10-20
    NDC Exclude Flag N
    Pricing Information N/A