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    NDC 71335-0097-03 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 Bryant Ranch Prepack. The primary component is VALSARTAN.

    Product Information

    NDC 71335-0097
    Product ID 71335-0097_fb3ef419-fb3b-4a40-9151-938741d26ade
    Associated GPIs 36150080000330
    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 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 Bryant Ranch Prepack
    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 2023-12-31

    Package

    NDC 71335-0097-03 (71335009703)

    NDC Package Code 71335-0097-3
    Billing NDC 71335009703
    Package 120 TABLET, FILM COATED in 1 BOTTLE (71335-0097-3)
    Marketing Start Date 2021-12-27
    NDC Exclude Flag N
    Pricing Information N/A