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    NDC 71335-0389-02 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 Bryant Ranch Prepack. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 71335-0389
    Product ID 71335-0389_3b92744f-99a2-4670-b6f6-ce35e7a23d11
    Associated GPIs 34000003100330
    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 5
    Active Ingredient Units mg/1
    Substance Name AMLODIPINE BESYLATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203245
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0389-02 (71335038902)

    NDC Package Code 71335-0389-2
    Billing NDC 71335038902
    Package 90 TABLET in 1 BOTTLE (71335-0389-2)
    Marketing Start Date 2020-06-25
    NDC Exclude Flag N
    Pricing Information N/A