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    NDC 51754-2005-01 Potassium Acetate 100 meq/50mL Details

    Potassium Acetate 100 meq/50mL

    Potassium Acetate is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Exela Pharma Sciences, LLC. The primary component is POTASSIUM ACETATE.

    Product Information

    NDC 51754-2005
    Product ID 51754-2005_2b86b9e8-48ba-4a72-b705-48c2751016e6
    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 Potassium Acetate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Potassium Acetate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAVENOUS
    Active Ingredient Strength 100
    Active Ingredient Units meq/50mL
    Substance Name POTASSIUM ACETATE
    Labeler Name Exela Pharma Sciences, LLC
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212692
    Listing Certified Through 2024-12-31

    Package

    NDC 51754-2005-01 (51754200501)

    NDC Package Code 51754-2005-1
    Billing NDC 51754200501
    Package 1 VIAL, GLASS in 1 CARTON (51754-2005-1) / 50 mL in 1 VIAL, GLASS
    Marketing Start Date 2022-03-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 51754-2004-04 51754-2005-04 >>

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