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    NDC 72789-0260-90 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 72789-0260
    Product ID 72789-260_0e7707c5-ca6a-e9fe-e063-6394a90a36e0
    Associated GPIs
    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 2.5 mg
    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 ANDA078414
    Listing Certified Through 2025-12-31

    Package

    NDC 72789-0260-90 (72789026090)

    NDC Package Code 72789-260-90
    Billing NDC 72789026090
    Package 90 TABLET in 1 BOTTLE, PLASTIC (72789-260-90)
    Marketing Start Date 2022-07-15
    NDC Exclude Flag N
    Pricing Information N/A