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    NDC 68788-7737-03 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 Preferred Pharmaceuticals, Inc.. The primary component is LOSARTAN POTASSIUM.

    Product Information

    NDC 68788-7737
    Product ID 68788-7737_c0d8c580-365c-4cee-b441-cbf8c2ae8871
    Associated GPIs 36150040200320
    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 25
    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 ANDA203835
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7737-03 (68788773703)

    NDC Package Code 68788-7737-3
    Billing NDC 68788773703
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-7737-3)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A