Search by Drug Name or NDC

    NDC 63629-8982-01 Ciprofloxacin 500 mg/1 Details

    Ciprofloxacin 500 mg/1

    Ciprofloxacin is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CIPROFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 63629-8982
    Product ID 63629-8982_e036a604-8842-4742-864e-7ea14b990725
    Associated GPIs
    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, COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name CIPROFLOXACIN HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208921
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-8982-01 (63629898201)

    NDC Package Code 63629-8982-1
    Billing NDC 63629898201
    Package 300 TABLET, COATED in 1 BOTTLE (63629-8982-1)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A