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    NDC 70518-3305-01 Losartan Potassium 50 mg/1 Details

    Losartan Potassium 50 mg/1

    Losartan Potassium is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is LOSARTAN POTASSIUM.

    Product Information

    NDC 70518-3305
    Product ID 70518-3305_0d815da9-3a00-c9f8-e063-6294a90a6752
    Associated GPIs
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name LOSARTAN POTASSIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090428
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3305-01 (70518330501)

    NDC Package Code 70518-3305-1
    Billing NDC 70518330501
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3305-1)
    Marketing Start Date 2022-06-06
    NDC Exclude Flag N
    Pricing Information N/A