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    NDC 61442-0224-50 Ciprofloxacin 750 mg/1 Details

    Ciprofloxacin 750 mg/1

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

    Product Information

    NDC 61442-0224
    Product ID 61442-224_592f5504-fe8f-36e4-e053-2991aa0a2347
    Associated GPIs 05000020100320
    GCN Sequence Number 009511
    GCN Sequence Number Description ciprofloxacin HCl TABLET 750 MG ORAL
    HIC3 W1Q
    HIC3 Description QUINOLONE ANTIBIOTICS
    GCN 47052
    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 Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Carlsbad Technology, Inc.
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076126
    Listing Certified Through 2023-12-31

    Package

    NDC 61442-0224-50 (61442022450)

    NDC Package Code 61442-224-50
    Billing NDC 61442022450
    Package 50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)
    Marketing Start Date 2009-10-10
    NDC Exclude Flag N
    Pricing Information N/A