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    NDC 71335-1747-01 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 Bryant Ranch Prepack. The primary component is POTASSIUM CHLORIDE.

    Product Information

    NDC 71335-1747
    Product ID 71335-1747_fdf3e671-7d42-cca8-e053-6294a90a277e
    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 Bryant Ranch Prepack
    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 71335-1747-01 (71335174701)

    NDC Package Code 71335-1747-1
    Billing NDC 71335174701
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-1)
    Marketing Start Date 2020-12-17
    NDC Exclude Flag N
    Pricing Information N/A