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    NDC 68382-0861-01 Potassium Chloride 750 mg/1 Details

    Potassium Chloride 750 mg/1

    Potassium Chloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals (USA) Inc.. The primary component is POTASSIUM CHLORIDE.

    Product Information

    NDC 68382-0861
    Product ID 68382-861_5e98c67f-9957-446f-bcf6-4ed08def954f
    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 750
    Active Ingredient Units mg/1
    Substance Name POTASSIUM CHLORIDE
    Labeler Name Zydus Pharmaceuticals (USA) Inc.
    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 ANDA210395
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0861-01 (68382086101)

    NDC Package Code 68382-861-01
    Billing NDC 68382086101
    Package 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-861-01)
    Marketing Start Date 2022-02-03
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 31e02249-7984-4b8f-9e37-2b79b708ac08 Details

    Revised: 10/2022