Search by Drug Name or NDC

    NDC 68788-7905-02 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 Preferred Pharmaceuticals Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 68788-7905
    Product ID 68788-7905_7e34396c-570e-4db0-91f2-3886424bc1f8
    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
    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 Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076558
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7905-02 (68788790502)

    NDC Package Code 68788-7905-2
    Billing NDC 68788790502
    Package 20 TABLET, FILM COATED in 1 BOTTLE (68788-7905-2)
    Marketing Start Date 2021-05-18
    NDC Exclude Flag N
    Pricing Information N/A