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    NDC 00121-1746-40 LACTULOSE 20 g/30mL Details

    LACTULOSE 20 g/30mL

    LACTULOSE is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pharmaceutical Associates, Inc.. The primary component is LACTULOSE.

    Product Information

    NDC 00121-1746
    Product ID 0121-1746_f0597d2a-6162-74d7-e053-2995a90a9894
    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 LACTULOSE
    Proprietary Name Suffix n/a
    Non-Proprietary Name LACTULOSE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units g/30mL
    Substance Name LACTULOSE
    Labeler Name Pharmaceutical Associates, Inc.
    Pharmaceutical Class Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074623
    Listing Certified Through 2024-12-31

    Package

    NDC 00121-1746-40 (00121174640)

    NDC Package Code 0121-1746-40
    Billing NDC 00121174640
    Package 4 TRAY in 1 CASE (0121-1746-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)
    Marketing Start Date 2019-12-03
    NDC Exclude Flag N
    Pricing Information N/A