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    NDC 68788-9012-08 ciprofloxacin 500 mg/1 Details

    ciprofloxacin 500 mg/1

    ciprofloxacin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 68788-9012
    Product ID 68788-9012_99fe21ea-3a82-44fb-963a-4916c3be5d01
    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
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    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 ANDA076639
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-9012-08 (68788901208)

    NDC Package Code 68788-9012-8
    Billing NDC 68788901208
    Package 10 TABLET in 1 BOTTLE (68788-9012-8)
    Marketing Start Date 2004-09-10
    NDC Exclude Flag N
    Pricing Information N/A