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    NDC 68788-8189-01 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 Preferred Pharmaceuticals Inc.. The primary component is LOSARTAN POTASSIUM.

    Product Information

    NDC 68788-8189
    Product ID 68788-8189_e4aecef2-0fa1-41b7-b0a0-36123c90392c
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name LOSARTAN POTASSIUM
    Labeler Name Preferred 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 68788-8189-01 (68788818901)

    NDC Package Code 68788-8189-1
    Billing NDC 68788818901
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68788-8189-1)
    Marketing Start Date 2022-05-13
    NDC Exclude Flag N
    Pricing Information N/A