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    NDC 70529-0136-02 Amphenol-40 9 mg/mL Details

    Amphenol-40 9 mg/mL

    Amphenol-40 is a INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by IT3 Medical LLC. The primary component is SODIUM CHLORIDE.

    Product Information

    NDC 70529-0136
    Product ID 70529-136_d8052160-e884-42d8-b50a-f0d2c694305d
    Associated GPIs 90948010101930
    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 Amphenol-40
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sodium Chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 9
    Active Ingredient Units mg/mL
    Substance Name SODIUM CHLORIDE
    Labeler Name IT3 Medical LLC
    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 AUTHORIZED GENERIC
    Application Number NDA018803
    Listing Certified Through 2023-12-31

    Package

    NDC 70529-0136-02 (70529013602)

    NDC Package Code 70529-136-02
    Billing NDC 70529013602
    Package 1 VIAL, SINGLE-DOSE in 1 PACKAGE (70529-136-02) / 10 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2017-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cbcdc635-ab36-46a0-af69-6f6d0c5f6ebb Details

    Revised: 2/2022