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    NDC 00338-0691-04 Potassium Chloride in Sodium Chloride 150; 900 mg/100mL; mg/100mL Details

    Potassium Chloride in Sodium Chloride 150; 900 mg/100mL; mg/100mL

    Potassium Chloride in Sodium Chloride is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is POTASSIUM CHLORIDE; SODIUM CHLORIDE.

    Product Information

    NDC 00338-0691
    Product ID 0338-0691_fea3418a-bd23-4b09-a318-c56c4c0eb31a
    Associated GPIs 79992002102020
    GCN Sequence Number 001198
    GCN Sequence Number Description potassium chloride in 0.9%NaCl IV SOLN 20 MEQ/L INTRAVEN
    HIC3 C1D
    HIC3 Description POTASSIUM REPLACEMENT
    GCN 56590
    HICL Sequence Number 014772
    HICL Sequence Number Description POTASSIUM CHLORIDE IN 0.9 % SODIUM CHLORIDE
    Brand/Generic Generic
    Proprietary Name Potassium Chloride in Sodium Chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Potassium Chloride and Sodium Chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 150; 900
    Active Ingredient Units mg/100mL; mg/100mL
    Substance Name POTASSIUM CHLORIDE; SODIUM CHLORIDE
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA],
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA017648
    Listing Certified Through 2024-12-31

    Package

    NDC 00338-0691-04 (00338069104)

    NDC Package Code 0338-0691-04
    Billing NDC 00338069104
    Package 14 BAG in 1 CARTON (0338-0691-04) / 1000 mL in 1 BAG
    Marketing Start Date 1979-02-02
    NDC Exclude Flag N
    Pricing Information N/A