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    NDC 70518-3035-01 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 REMEDYREPACK INC.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 70518-3035
    Product ID 70518-3035_0e8940d5-0fd4-d33b-e063-6294a90a5c79
    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, COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK 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 2025-12-31

    Package

    NDC 70518-3035-01 (70518303501)

    NDC Package Code 70518-3035-1
    Billing NDC 70518303501
    Package 30 TABLET, COATED in 1 BLISTER PACK (70518-3035-1)
    Marketing Start Date 2024-01-09
    NDC Exclude Flag N
    Pricing Information N/A