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    NDC 70934-0603-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is NIFEDIPINE.

    Product Information

    NDC 70934-0603
    Product ID 70934-603_d7316650-c4f6-2ce6-e053-2995a90ad286
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203126
    Listing Certified Through n/a

    Package

    NDC 70934-0603-30 (70934060330)

    NDC Package Code 70934-603-30
    Billing NDC 70934060330
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-603-30)
    Marketing Start Date 2020-03-05
    NDC Exclude Flag N
    Pricing Information N/A
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