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    NDC 00955-1057-30 Sevelamer Carbonate 800 mg/1 Details

    Sevelamer Carbonate 800 mg/1

    Sevelamer Carbonate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Winthrop U.S, a business of sanofi-aventis U.S. LLC. The primary component is SEVELAMER CARBONATE.

    Product Information

    NDC 00955-1057
    Product ID 0955-1057_0bef7188-5f19-0981-e063-6294a90a1881
    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 Sevelamer Carbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sevelamer Carbonate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 800
    Active Ingredient Units mg/1
    Substance Name SEVELAMER CARBONATE
    Labeler Name Winthrop U.S, a business of sanofi-aventis U.S. LLC
    Pharmaceutical Class Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA022127
    Listing Certified Through 2024-12-31

    Package

    NDC 00955-1057-30 (00955105730)

    NDC Package Code 0955-1057-30
    Billing NDC 00955105730
    Package 270 TABLET, FILM COATED in 1 BOTTLE (0955-1057-30)
    Marketing Start Date 2023-07-14
    NDC Exclude Flag N
    Pricing Information N/A