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    NDC 70934-0075-90 Amlodipine Besylate 5 mg/1 Details

    Amlodipine Besylate 5 mg/1

    Amlodipine Besylate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 70934-0075
    Product ID 70934-075_f14f3ee5-2f4d-cb43-e053-2995a90adfea
    Associated GPIs 34000003100330
    GCN Sequence Number 016926
    GCN Sequence Number Description amlodipine besylate TABLET 5 MG ORAL
    HIC3 A9A
    HIC3 Description CALCIUM CHANNEL BLOCKING AGENTS
    GCN 02683
    HICL Sequence Number 006494
    HICL Sequence Number Description AMLODIPINE BESYLATE
    Brand/Generic Generic
    Proprietary Name Amlodipine Besylate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amlodipine besylate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name AMLODIPINE BESYLATE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078925
    Listing Certified Through n/a

    Package

    NDC 70934-0075-90 (70934007590)

    NDC Package Code 70934-075-90
    Billing NDC 70934007590
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70934-075-90)
    Marketing Start Date 2018-12-12
    NDC Exclude Flag N
    Pricing Information N/A