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    NDC 59762-6723-01 Amlodipine besylate and Atorvastatin calcium 5; 80 mg/1; mg/1 Details

    Amlodipine besylate and Atorvastatin calcium 5; 80 mg/1; mg/1

    Amlodipine besylate and Atorvastatin calcium is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Greenstone LLC. The primary component is AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 59762-6723
    Product ID 59762-6723_f5bda790-fb33-4fee-88cf-cd45581f2b81
    Associated GPIs 40992502150335
    GCN Sequence Number 053692
    GCN Sequence Number Description amlodipine/atorvastatin TABLET 5 MG-80 MG ORAL
    HIC3 M4I
    HIC3 Description ANTIHYPERLIPID- HMG-COA RI-CALCIUM CHANNEL BLOCKER
    GCN 21394
    HICL Sequence Number 025951
    HICL Sequence Number Description AMLODIPINE BESYLATE/ATORVASTATIN CALCIUM
    Brand/Generic Generic
    Proprietary Name Amlodipine besylate and Atorvastatin calcium
    Proprietary Name Suffix n/a
    Non-Proprietary Name amlodipine besylate and atorvastatin calcium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 80
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
    Labeler Name Greenstone LLC
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA021540
    Listing Certified Through 2024-12-31

    Package

    NDC 59762-6723-01 (59762672301)

    NDC Package Code 59762-6723-1
    Billing NDC 59762672301
    Package 30 TABLET, FILM COATED in 1 BOTTLE (59762-6723-1)
    Marketing Start Date 2014-04-04
    NDC Exclude Flag N
    Pricing Information N/A