Search by Drug Name or NDC

    NDC 70518-2981-00 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 REMEDYREPACK INC.. The primary component is AMLODIPINE BESYLATE.

    Product Information

    NDC 70518-2981
    Product ID 70518-2981_0c8d5aa8-b21e-c7b9-e063-6294a90a566e
    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 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 70518-2981-00 (70518298100)

    NDC Package Code 70518-2981-0
    Billing NDC 70518298100
    Package 30 TABLET in 1 BLISTER PACK (70518-2981-0)
    Marketing Start Date 2021-01-06
    NDC Exclude Flag N
    Pricing Information N/A