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    NDC 61919-0009-90 MONTELUKAST SODIUM 10 mg/1 Details

    MONTELUKAST SODIUM 10 mg/1

    MONTELUKAST SODIUM is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECT RX. The primary component is MONTELUKAST SODIUM.

    Product Information

    NDC 61919-0009
    Product ID 61919-009_f200a4c8-a6d4-86e0-e053-2a95a90a5a4e
    Associated GPIs 44505050100330
    GCN Sequence Number 038451
    GCN Sequence Number Description montelukast sodium TABLET 10 MG ORAL
    HIC3 Z4B
    HIC3 Description LEUKOTRIENE RECEPTOR ANTAGONISTS
    GCN 94444
    HICL Sequence Number 016911
    HICL Sequence Number Description MONTELUKAST SODIUM
    Brand/Generic Generic
    Proprietary Name MONTELUKAST SODIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name MONTELUKAST SODIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name MONTELUKAST SODIUM
    Labeler Name DIRECT RX
    Pharmaceutical Class Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202717
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0009-90 (61919000990)

    NDC Package Code 61919-009-90
    Billing NDC 61919000990
    Package 90 TABLET, FILM COATED in 1 BOTTLE (61919-009-90)
    Marketing Start Date 2015-01-01
    NDC Exclude Flag N
    Pricing Information N/A