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    NDC 10122-0103-05 FERRIPROX 1000 mg/1 Details

    FERRIPROX 1000 mg/1

    FERRIPROX is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chiesi USA, Inc.. The primary component is DEFERIPRONE.

    Product Information

    NDC 10122-0103
    Product ID 10122-103_4f6573ca-2d61-4602-8a51-f9e30af2e489
    Associated GPIs 93100028000340
    GCN Sequence Number 067196
    GCN Sequence Number Description deferiprone TABLET 1000 MG ORAL
    HIC3 C8A
    HIC3 Description METALLIC POISON,AGENTS TO TREAT
    GCN 29687
    HICL Sequence Number 018544
    HICL Sequence Number Description DEFERIPRONE
    Brand/Generic Brand
    Proprietary Name FERRIPROX
    Proprietary Name Suffix n/a
    Non-Proprietary Name DEFERIPRONE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 1000
    Active Ingredient Units mg/1
    Substance Name DEFERIPRONE
    Labeler Name Chiesi USA, Inc.
    Pharmaceutical Class Iron Chelating Activity [MoA], Iron Chelator [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021825
    Listing Certified Through 2024-12-31

    Package

    NDC 10122-0103-05 (10122010305)

    NDC Package Code 10122-103-05
    Billing NDC 10122010305
    Package 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-103-05)
    Marketing Start Date 2019-08-01
    NDC Exclude Flag N
    Pricing Information N/A