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    NDC 68788-7642-09 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 Preferred Pharmaceuticals, Inc.. The primary component is NIFEDIPINE.

    Product Information

    NDC 68788-7642
    Product ID 68788-7642_50a36e7a-1abc-441e-b1ef-f166e72063ae
    Associated GPIs 34000020007570
    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 30
    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 68788-7642-09 (68788764209)

    NDC Package Code 68788-7642-9
    Billing NDC 68788764209
    Package 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)
    Marketing Start Date 2020-02-28
    NDC Exclude Flag N
    Pricing Information N/A