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    NDC 53002-1638-00 Losartan Potassium 100 mg/1 Details

    Losartan Potassium 100 mg/1

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

    Product Information

    NDC 53002-1638
    Product ID 53002-1638_167c22f2-f172-4595-b850-1e523c8afa82
    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 100
    Active Ingredient Units mg/1
    Substance Name LOSARTAN POTASSIUM
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091497
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1638-00 (53002163800)

    NDC Package Code 53002-1638-0
    Billing NDC 53002163800
    Package 100 TABLET, FILM COATED in 1 BOTTLE (53002-1638-0)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A