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    NDC 51655-0118-84 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 Northwind Pharmaceuticals, LLC. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 51655-0118
    Product ID 51655-118_063163ca-25d9-6156-e063-6294a90a949f
    Associated GPIs
    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 Northwind Pharmaceuticals, LLC
    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 2025-12-31

    Package

    NDC 51655-0118-84 (51655011884)

    NDC Package Code 51655-118-84
    Billing NDC 51655011884
    Package 14 TABLET in 1 BOTTLE, DISPENSING (51655-118-84)
    Marketing Start Date 2014-06-01
    NDC Exclude Flag N
    Pricing Information N/A