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    NDC 69117-0009-01 Ciprofloxacin 500 mg/1 Details

    Ciprofloxacin 500 mg/1

    Ciprofloxacin is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Yiling Pharmaceutical, Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 69117-0009
    Product ID 69117-0009_0da6e293-914e-3146-e063-6394a90a0399
    Associated GPIs 05000020100315
    GCN Sequence Number 009510
    GCN Sequence Number Description ciprofloxacin HCl TABLET 500 MG ORAL
    HIC3 W1Q
    HIC3 Description QUINOLONE ANTIBIOTICS
    GCN 47051
    HICL Sequence Number 004124
    HICL Sequence Number Description CIPROFLOXACIN HCL
    Brand/Generic Generic
    Proprietary Name Ciprofloxacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ciprofloxacin Tablets
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Yiling Pharmaceutical, 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 69117-0009-01 (69117000901)

    NDC Package Code 69117-0009-1
    Billing NDC 69117000901
    Package 500 TABLET, COATED in 1 BOTTLE (69117-0009-1)
    Marketing Start Date 2019-07-13
    NDC Exclude Flag N
    Pricing Information N/A