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    NDC 55111-0733-78 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 Dr. Reddy's Laboratories Limited. The primary component is VALSARTAN.

    Product Information

    NDC 55111-0733
    Product ID 55111-733_48e7d0aa-d6a3-6f6d-cea1-68cb64bc45c1
    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 Dr. Reddy's Laboratories Limited
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201618
    Listing Certified Through 2024-12-31

    Package

    NDC 55111-0733-78 (55111073378)

    NDC Package Code 55111-733-78
    Billing NDC 55111073378
    Package 10 BLISTER PACK in 1 CARTON (55111-733-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-733-79)
    Marketing Start Date 2021-10-05
    NDC Exclude Flag N
    Pricing Information N/A