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    NDC 62135-0192-22 Calcium Acetate 667 mg/1 Details

    Calcium Acetate 667 mg/1

    Calcium Acetate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX LLC. The primary component is CALCIUM ACETATE.

    Product Information

    NDC 62135-0192
    Product ID 62135-192_f049c4ca-c996-fa6c-e053-2995a90a42bf
    Associated GPIs 52800020100320
    GCN Sequence Number 027508
    GCN Sequence Number Description calcium acetate TABLET 667 MG ORAL
    HIC3 C1A
    HIC3 Description ELECTROLYTE DEPLETERS
    GCN 75051
    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 TABLET
    Route ORAL
    Active Ingredient Strength 667
    Active Ingredient Units mg/1
    Substance Name CALCIUM ACETATE
    Labeler Name Chartwell RX LLC
    Pharmaceutical Class Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202420
    Listing Certified Through 2024-12-31

    Package

    NDC 62135-0192-22 (62135019222)

    NDC Package Code 62135-192-22
    Billing NDC 62135019222
    Package 200 TABLET in 1 BOTTLE (62135-192-22)
    Marketing Start Date 2019-07-01
    NDC Exclude Flag N
    Pricing Information N/A