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    NDC 68788-8136-01 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 Preferred Pharmaceuticals Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 68788-8136
    Product ID 68788-8136_8413e0fa-b71d-4ed2-b2c2-34e305244f7b
    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 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 Preferred Pharmaceuticals 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 68788-8136-01 (68788813601)

    NDC Package Code 68788-8136-1
    Billing NDC 68788813601
    Package 14 TABLET, FILM COATED in 1 BOTTLE (68788-8136-1)
    Marketing Start Date 2022-02-03
    NDC Exclude Flag N
    Pricing Information N/A