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    NDC 70934-0316-30 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 70934-0316
    Product ID 70934-316_f1756152-0021-bdea-e053-2a95a90ae346
    Associated GPIs 05000020100315
    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
    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 ANDA075593
    Listing Certified Through n/a

    Package

    NDC 70934-0316-30 (70934031630)

    NDC Package Code 70934-316-30
    Billing NDC 70934031630
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-316-30)
    Marketing Start Date 2021-01-22
    NDC Exclude Flag N
    Pricing Information N/A