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    NDC 62332-0208-10 Amlodipine and Valsartan 10; 320 mg/1; mg/1 Details

    Amlodipine and Valsartan 10; 320 mg/1; mg/1

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

    Product Information

    NDC 62332-0208
    Product ID 62332-208_22831006-efb4-495c-9dfd-c2deab13d40c
    Associated GPIs 36993002100340
    GCN Sequence Number 062809
    GCN Sequence Number Description amlodipine besylate/valsartan TABLET 10MG-320MG ORAL
    HIC3 A4H
    HIC3 Description ANGIOTENSIN RECEPTOR BLOCKR-CALCIUM CHANNEL BLOCKR
    GCN 98580
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 10; 320
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; VALSARTAN
    Labeler Name Alembic 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 ANDA202713
    Listing Certified Through 2024-12-31

    Package

    NDC 62332-0208-10 (62332020810)

    NDC Package Code 62332-208-10
    Billing NDC 62332020810
    Package 100 TABLET, FILM COATED in 1 CARTON (62332-208-10)
    Marketing Start Date 2016-12-01
    NDC Exclude Flag N
    Pricing Information N/A