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    NDC 70934-0093-20 Ciprofloxacin 500 mg/1 Details

    Ciprofloxacin 500 mg/1

    Ciprofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 70934-0093
    Product ID 70934-093_d244c753-8a4a-c362-e053-2995a90a7e1b
    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 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 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077859
    Listing Certified Through n/a

    Package

    NDC 70934-0093-20 (70934009320)

    NDC Package Code 70934-093-20
    Billing NDC 70934009320
    Package 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-20)
    Marketing Start Date 2020-11-06
    NDC Exclude Flag N
    Pricing Information N/A