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    NDC 70518-1971-01 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 REMEDYREPACK INC.. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 70518-1971
    Product ID 70518-1971_03705afb-8c67-2cb3-e063-6294a90a6aa9
    Associated GPIs 34000003100320
    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 2.5
    Active Ingredient Units mg/1
    Substance Name AMLODIPINE BESYLATE
    Labeler Name REMEDYREPACK 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 ANDA078925
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1971-01 (70518197101)

    NDC Package Code 70518-1971-1
    Billing NDC 70518197101
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70518-1971-1)
    Marketing Start Date 2019-07-15
    NDC Exclude Flag N
    Pricing Information N/A