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    NDC 72789-0125-50 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 PD-Rx Pharmaceuticals, Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 72789-0125
    Product ID 72789-125_f29147c8-4ac3-3e85-e053-2a95a90a9a19
    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
    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 PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076558
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0125-50 (72789012550)

    NDC Package Code 72789-125-50
    Billing NDC 72789012550
    Package 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-125-50)
    Marketing Start Date 2020-10-07
    NDC Exclude Flag N
    Pricing Information N/A