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    NDC 71335-0181-03 Losartan Potassium 50 mg/1 Details

    Losartan Potassium 50 mg/1

    Losartan Potassium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is LOSARTAN POTASSIUM.

    Product Information

    NDC 71335-0181
    Product ID 71335-0181_a0c24b4a-8137-48e9-bc01-1e644055a04f
    Associated GPIs 36150040200330
    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 Losartan Potassium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Losartan Potassium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name LOSARTAN POTASSIUM
    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 ANDA090467
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0181-03 (71335018103)

    NDC Package Code 71335-0181-3
    Billing NDC 71335018103
    Package 60 TABLET in 1 BOTTLE (71335-0181-3)
    Marketing Start Date 2022-05-02
    NDC Exclude Flag N
    Pricing Information N/A