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    NDC 55154-4690-00 Nifedipine 30 mg/1 Details

    Nifedipine 30 mg/1

    Nifedipine is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is NIFEDIPINE.

    Product Information

    NDC 55154-4690
    Product ID 55154-4690_29d3e753-7841-4aff-9f56-1b3bbad8b08e
    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 Nifedipine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Nifedipine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name NIFEDIPINE
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077127
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-4690-00 (55154469000)

    NDC Package Code 55154-4690-0
    Billing NDC 55154469000
    Package 10 BLISTER PACK in 1 BAG (55154-4690-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2012-05-24
    NDC Exclude Flag N
    Pricing Information N/A