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    NDC 70518-0932-00 Levofloxacin 750 mg/1 Details

    Levofloxacin 750 mg/1

    Levofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is LEVOFLOXACIN.

    Product Information

    NDC 70518-0932
    Product ID 70518-0932_0d6bf85c-3b4f-4b8d-e063-6294a90a728e
    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 Levofloxacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Levofloxacin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name LEVOFLOXACIN
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076710
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-0932-00 (70518093200)

    NDC Package Code 70518-0932-0
    Billing NDC 70518093200
    Package 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0932-0)
    Marketing Start Date 2018-01-05
    NDC Exclude Flag N
    Pricing Information N/A