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    NDC 62135-0311-06 Ciprofloxacin 100 mg/1 Details

    Ciprofloxacin 100 mg/1

    Ciprofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 62135-0311
    Product ID 62135-311_f2a0db9f-16a8-1603-e053-2995a90a79a3
    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 hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Chartwell RX, LLC.
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076896
    Listing Certified Through 2024-12-31

    Package

    NDC 62135-0311-06 (62135031106)

    NDC Package Code 62135-311-06
    Billing NDC 62135031106
    Package 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-311-06)
    Marketing Start Date 2022-04-20
    NDC Exclude Flag N
    Pricing Information N/A