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    NDC 51655-0568-90 Potassium Chloride 1500 mg/1 Details

    Potassium Chloride 1500 mg/1

    Potassium Chloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is POTASSIUM CHLORIDE.

    Product Information

    NDC 51655-0568
    Product ID 51655-568_dae7c63d-eef1-58d0-e053-2a95a90a667e
    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 Chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name potassium chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1500
    Active Ingredient Units mg/1
    Substance Name POTASSIUM CHLORIDE
    Labeler Name Northwind Pharmaceuticals, 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 ANDA074726
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0568-90 (51655056890)

    NDC Package Code 51655-568-90
    Billing NDC 51655056890
    Package 45 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-90)
    Marketing Start Date 2023-03-06
    NDC Exclude Flag N
    Pricing Information N/A