Search by Drug Name or NDC

    NDC 70954-0197-20 Potassium chloride 1.5 g/1.56g Details

    Potassium chloride 1.5 g/1.56g

    Potassium chloride is a ORAL FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ANI Pharmaceuticals, Inc.. The primary component is POTASSIUM CHLORIDE.

    Product Information

    NDC 70954-0197
    Product ID 70954-197_0128a879-7185-4b70-b0bb-d108ff1c9542
    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 FOR SOLUTION
    Route ORAL
    Active Ingredient Strength 1.5
    Active Ingredient Units g/1.56g
    Substance Name POTASSIUM CHLORIDE
    Labeler Name ANI Pharmaceuticals, 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 ANDA212816
    Listing Certified Through 2024-12-31

    Package

    NDC 70954-0197-20 (70954019720)

    NDC Package Code 70954-197-20
    Billing NDC 70954019720
    Package 30 POUCH in 1 CARTON (70954-197-20) / 1.56 g in 1 POUCH (70954-197-10)
    Marketing Start Date 2023-07-19
    NDC Exclude Flag N
    Pricing Information N/A
    << 70954-0188-10 70954-0197-30 >>

    Contents