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    NDC 68071-2205-09 LOSARTAN POTASSIUM 25 mg/1 Details

    LOSARTAN POTASSIUM 25 mg/1

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

    Product Information

    NDC 68071-2205
    Product ID 68071-2205_0075774d-9b16-7e25-e063-6394a90a0fc1
    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 25 mg
    Non-Proprietary Name LOSARTAN POTASSIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name LOSARTAN POTASSIUM
    Labeler Name NuCare Pharmaceuticals,Inc.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090382
    Listing Certified Through 2024-12-31

    Package

    NDC 68071-2205-09 (68071220509)

    NDC Package Code 68071-2205-9
    Billing NDC 68071220509
    Package 90 TABLET, FILM COATED in 1 BOTTLE (68071-2205-9)
    Marketing Start Date 2020-07-06
    NDC Exclude Flag N
    Pricing Information N/A