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    NDC 00338-9537-50 SODIUM CHLORIDE 900 mg/100mL Details

    SODIUM CHLORIDE 900 mg/100mL

    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 SODIUM CHLORIDE.

    Product Information

    NDC 00338-9537
    Product ID 0338-9537_c97c667c-1fee-4e13-be78-eb2b3f072c5c
    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 SODIUM CHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name sodium chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 900
    Active Ingredient Units mg/100mL
    Substance Name SODIUM CHLORIDE
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA016677
    Listing Certified Through 2022-12-31

    Package

    NDC 00338-9537-50 (00338953750)

    NDC Package Code 0338-9537-50
    Billing NDC 00338953750
    Package 50 BAG in 1 CARTON (0338-9537-50) / 100 mL in 1 BAG
    Marketing Start Date 2018-03-09
    NDC Exclude Flag N
    Pricing Information N/A