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    NDC 50419-0754-01 Cipro 500 mg/1 Details

    Cipro 500 mg/1

    Cipro is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bayer HealthCare Pharmaceuticals Inc.. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 50419-0754
    Product ID 50419-754_d4987631-55b6-49e8-9281-3fa55a7c13b3
    Associated GPIs 05000020100315
    GCN Sequence Number 009510
    GCN Sequence Number Description ciprofloxacin HCl TABLET 500 MG ORAL
    HIC3 W1Q
    HIC3 Description QUINOLONE ANTIBIOTICS
    GCN 47051
    HICL Sequence Number 004124
    HICL Sequence Number Description CIPROFLOXACIN HCL
    Brand/Generic Brand
    Proprietary Name Cipro
    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 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Bayer HealthCare Pharmaceuticals Inc.
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA019537
    Listing Certified Through 2024-12-31

    Package

    NDC 50419-0754-01 (50419075401)

    NDC Package Code 50419-754-01
    Billing NDC 50419075401
    Package 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01)
    Marketing Start Date 1987-10-22
    NDC Exclude Flag N
    Pricing Information N/A