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    NDC 43063-0764-30 AMLODIPINE BESYLATE 2.5 mg/1 Details

    AMLODIPINE BESYLATE 2.5 mg/1

    AMLODIPINE BESYLATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 43063-0764
    Product ID 43063-764_06593e4f-fde6-361b-e063-6394a90a3a3e
    Associated GPIs 34000003100320
    GCN Sequence Number 016925
    GCN Sequence Number Description amlodipine besylate TABLET 2.5 MG ORAL
    HIC3 A9A
    HIC3 Description CALCIUM CHANNEL BLOCKING AGENTS
    GCN 02681
    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 2.5
    Active Ingredient Units mg/1
    Substance Name AMLODIPINE BESYLATE
    Labeler Name PD-Rx Pharmaceuticals, 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 ANDA077073
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0764-30 (43063076430)

    NDC Package Code 43063-764-30
    Billing NDC 43063076430
    Package 30 TABLET in 1 BOTTLE, PLASTIC (43063-764-30)
    Marketing Start Date 2017-05-08
    NDC Exclude Flag N
    Pricing Information N/A