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    NDC 70934-0330-30 Amlodipine Besylate 10 mg/1 Details

    Amlodipine Besylate 10 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 70934-0330
    Product ID 70934-330_f14f3ee5-2f4c-cb43-e053-2995a90adfea
    Associated GPIs 34000003100340
    GCN Sequence Number 016927
    GCN Sequence Number Description amlodipine besylate TABLET 10 MG ORAL
    HIC3 A9A
    HIC3 Description CALCIUM CHANNEL BLOCKING AGENTS
    GCN 02682
    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 10
    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 70934-0330-30 (70934033030)

    NDC Package Code 70934-330-30
    Billing NDC 70934033030
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-330-30)
    Marketing Start Date 2019-03-27
    NDC Exclude Flag N
    Pricing Information N/A