Search by Drug Name or NDC

    NDC 68180-0766-09 Amlodipine and Valsartan 5; 320 mg/1; mg/1 Details

    Amlodipine and Valsartan 5; 320 mg/1; mg/1

    Amlodipine and Valsartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is AMLODIPINE BESYLATE; VALSARTAN.

    Product Information

    NDC 68180-0766
    Product ID 68180-766_e0777a79-35ef-4f69-b6ac-94d31f7ca6fb
    Associated GPIs 36993002100320
    GCN Sequence Number 062808
    GCN Sequence Number Description amlodipine besylate/valsartan TABLET 5 MG-320MG ORAL
    HIC3 A4H
    HIC3 Description ANGIOTENSIN RECEPTOR BLOCKR-CALCIUM CHANNEL BLOCKR
    GCN 98579
    HICL Sequence Number 034433
    HICL Sequence Number Description AMLODIPINE BESYLATE/VALSARTAN
    Brand/Generic Generic
    Proprietary Name Amlodipine and Valsartan
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amlodipine and Valsartan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5; 320
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; VALSARTAN
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], 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 ANDA090245
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0766-09 (68180076609)

    NDC Package Code 68180-766-09
    Billing NDC 68180076609
    Package 90 TABLET in 1 BOTTLE (68180-766-09)
    Marketing Start Date 2015-03-31
    NDC Exclude Flag N
    Pricing Information N/A