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    NDC 65162-0590-50 Calcium Acetate 667 mg/1 Details

    Calcium Acetate 667 mg/1

    Calcium Acetate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is CALCIUM ACETATE.

    Product Information

    NDC 65162-0590
    Product ID 65162-590_f2c59635-97a7-4016-a443-0054d9e69225
    Associated GPIs 52800020100120
    GCN Sequence Number 048241
    GCN Sequence Number Description calcium acetate CAPSULE 667 MG ORAL
    HIC3 C1A
    HIC3 Description ELECTROLYTE DEPLETERS
    GCN 13675
    HICL Sequence Number 004884
    HICL Sequence Number Description CALCIUM ACETATE
    Brand/Generic Generic
    Proprietary Name Calcium Acetate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Calcium Acetate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 667
    Active Ingredient Units mg/1
    Substance Name CALCIUM ACETATE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201658
    Listing Certified Through 2024-12-31

    Package

    NDC 65162-0590-50 (65162059050)

    NDC Package Code 65162-590-50
    Billing NDC 65162059050
    Package 500 CAPSULE in 1 BOTTLE (65162-590-50)
    Marketing Start Date 2014-10-08
    NDC Exclude Flag N
    Pricing Information N/A