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    NDC 00093-5939-98 Lanthanum carbonate 750 mg/1 Details

    Lanthanum carbonate 750 mg/1

    Lanthanum carbonate is a ORAL TABLET, CHEWABLE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Pharmaceuticals USA, Inc.. The primary component is LANTHANUM CARBONATE.

    Product Information

    NDC 00093-5939
    Product ID 0093-5939_c7a37d6c-c06f-440c-8c13-37508567f1fc
    Associated GPIs 52800045200550
    GCN Sequence Number 060097
    GCN Sequence Number Description lanthanum carbonate TAB CHEW 750 MG ORAL
    HIC3 C1A
    HIC3 Description ELECTROLYTE DEPLETERS
    GCN 26116
    HICL Sequence Number 026756
    HICL Sequence Number Description LANTHANUM CARBONATE
    Brand/Generic Generic
    Proprietary Name Lanthanum carbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lanthanum carbonate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name LANTHANUM CARBONATE
    Labeler Name Teva Pharmaceuticals USA, Inc.
    Pharmaceutical Class Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090977
    Listing Certified Through 2024-12-31

    Package

    NDC 00093-5939-98 (00093593998)

    NDC Package Code 0093-5939-98
    Billing NDC 00093593998
    Package 6 BOTTLE in 1 CARTON (0093-5939-98) / 15 TABLET, CHEWABLE in 1 BOTTLE (0093-5939-85)
    Marketing Start Date 2022-05-25
    NDC Exclude Flag N
    Pricing Information N/A