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    NDC 68788-8164-06 Nifedipine 60 mg/1 Details

    Nifedipine 60 mg/1

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

    Product Information

    NDC 68788-8164
    Product ID 68788-8164_ca07b9ff-53d7-42c4-8356-a65f497a3af3
    Associated GPIs 34000020007575
    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, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 60
    Active Ingredient Units mg/1
    Substance Name NIFEDIPINE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210614
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8164-06 (68788816406)

    NDC Package Code 68788-8164-6
    Billing NDC 68788816406
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8164-6)
    Marketing Start Date 2022-04-04
    NDC Exclude Flag N
    Pricing Information N/A