Search by Drug Name or NDC

    NDC 71335-0799-01 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 71335-0799
    Product ID 71335-0799_6b77fc51-31d5-4057-86a3-351674300a31
    Associated GPIs 34000003100340
    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], 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 71335-0799-01 (71335079901)

    NDC Package Code 71335-0799-1
    Billing NDC 71335079901
    Package 30 TABLET in 1 BOTTLE (71335-0799-1)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A