Search by Drug Name or NDC

    NDC 71335-1887-09 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 Bryant Ranch Prepack. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 71335-1887
    Product ID 71335-1887_42be4afb-caa4-4ad4-b489-bd42b182ea9c
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 Bryant Ranch Prepack
    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 71335-1887-09 (71335188709)

    NDC Package Code 71335-1887-9
    Billing NDC 71335188709
    Package 10 TABLET in 1 BOTTLE (71335-1887-9)
    Marketing Start Date 2022-02-15
    NDC Exclude Flag N
    Pricing Information N/A