Search by Drug Name or NDC

    NDC 33342-0064-15 Valsartan 160 mg/1 Details

    Valsartan 160 mg/1

    Valsartan is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Macleods Pharmaceuticals Limited. The primary component is VALSARTAN.

    Product Information

    NDC 33342-0064
    Product ID 33342-064_1fff1472-c659-469c-8786-f3c9b6689524
    Associated GPIs 36150080000330
    GCN Sequence Number 048400
    GCN Sequence Number Description valsartan TABLET 160 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 13844
    HICL Sequence Number 012204
    HICL Sequence Number Description VALSARTAN
    Brand/Generic Generic
    Proprietary Name Valsartan
    Proprietary Name Suffix n/a
    Non-Proprietary Name Valsartan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 160
    Active Ingredient Units mg/1
    Substance Name VALSARTAN
    Labeler Name Macleods Pharmaceuticals Limited
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202696
    Listing Certified Through 2024-12-31

    Package

    NDC 33342-0064-15 (33342006415)

    NDC Package Code 33342-064-15
    Billing NDC 33342006415
    Package 500 TABLET, FILM COATED in 1 BOTTLE (33342-064-15)
    Marketing Start Date 2016-09-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 251ccff4-bf86-453b-9d1c-e3c1ecfd3a46 Details

    Revised: 10/2022