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    NDC 68382-0854-10 potassium chloride 750 mg/1 Details

    potassium chloride 750 mg/1

    potassium chloride is a ORAL CAPSULE, 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 68382-0854
    Product ID 68382-854_37302db1-d7cc-4b79-8b3e-f14d40342ef4
    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 CAPSULE, 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 ANDA208445
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0854-10 (68382085410)

    NDC Package Code 68382-854-10
    Billing NDC 68382085410
    Package 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-854-10)
    Marketing Start Date 2019-06-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 51586c47-1aff-4ce6-8030-89f9eb1bc9ac Details

    Revised: 2/2021