Search by Drug Name or NDC

    NDC 71093-0147-05 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 ACI Healthcare USA, Inc.. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 71093-0147
    Product ID 71093-147_5a93579c-5d45-4662-b39c-8d93b04f52dc
    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 ACI Healthcare USA, Inc.
    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 ANDA077516
    Listing Certified Through 2024-12-31

    Package

    NDC 71093-0147-05 (71093014705)

    NDC Package Code 71093-147-05
    Billing NDC 71093014705
    Package 500 TABLET in 1 BOTTLE (71093-147-05)
    Marketing Start Date 2018-11-12
    NDC Exclude Flag N
    Pricing Information N/A