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    NDC 70518-2786-00 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 70518-2786
    Product ID 70518-2786_0d1f28e5-e5fb-6031-e063-6394a90a0815
    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 ANDA203835
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2786-00 (70518278600)

    NDC Package Code 70518-2786-0
    Billing NDC 70518278600
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2786-0)
    Marketing Start Date 2020-06-14
    NDC Exclude Flag N
    Pricing Information N/A