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    NDC 76282-0664-27 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 Exelan Pharmaceuticals Inc.. The primary component is SEVELAMER CARBONATE.

    Product Information

    NDC 76282-0664
    Product ID 76282-664_831095de-d22d-496d-834c-c4505e639c87
    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 Exelan Pharmaceuticals Inc.
    Pharmaceutical Class Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203860
    Listing Certified Through 2024-12-31

    Package

    NDC 76282-0664-27 (76282066427)

    NDC Package Code 76282-664-27
    Billing NDC 76282066427
    Package 270 TABLET, FILM COATED in 1 BOTTLE (76282-664-27)
    Marketing Start Date 2019-08-08
    NDC Exclude Flag N
    Pricing Information N/A