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    NDC 68788-8200-01 Ciprofloxacin 250 mg/1 Details

    Ciprofloxacin 250 mg/1

    Ciprofloxacin is a ORAL TABLET, 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 68788-8200
    Product ID 68788-8200_6c7d11ed-df40-498a-ba52-117e0b43c482
    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, 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 ANDA208921
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8200-01 (68788820001)

    NDC Package Code 68788-8200-1
    Billing NDC 68788820001
    Package 10 TABLET, COATED in 1 BOTTLE (68788-8200-1)
    Marketing Start Date 2022-05-24
    NDC Exclude Flag N
    Pricing Information N/A