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    NDC 68788-9006-02 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 68788-9006
    Product ID 68788-9006_ff470c89-9638-4e39-a5fa-aa0dfafdbe3e
    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 Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075593
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-9006-02 (68788900602)

    NDC Package Code 68788-9006-2
    Billing NDC 68788900602
    Package 20 TABLET, FILM COATED in 1 BOTTLE (68788-9006-2)
    Marketing Start Date 2011-06-14
    NDC Exclude Flag N
    Pricing Information N/A