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    NDC 63629-9109-01 Nifedipine 30 mg/1 Details

    Nifedipine 30 mg/1

    Nifedipine is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is NIFEDIPINE.

    Product Information

    NDC 63629-9109
    Product ID 63629-9109_21d4cbf3-f217-40ba-89e0-77e9539ceb02
    Associated GPIs
    GCN Sequence Number 012059
    GCN Sequence Number Description nifedipine TABLET ER 30 MG ORAL
    HIC3 A9A
    HIC3 Description CALCIUM CHANNEL BLOCKING AGENTS
    GCN 02226
    HICL Sequence Number 000181
    HICL Sequence Number Description NIFEDIPINE
    Brand/Generic Generic
    Proprietary Name Nifedipine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Nifedipine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name NIFEDIPINE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075269
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-9109-01 (63629910901)

    NDC Package Code 63629-9109-1
    Billing NDC 63629910901
    Package 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9109-1)
    Marketing Start Date 2023-02-16
    NDC Exclude Flag N
    Pricing Information N/A