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    NDC 43063-0854-90 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 PD-Rx Pharmaceuticals, Inc.. The primary component is LOSARTAN POTASSIUM.

    Product Information

    NDC 43063-0854
    Product ID 43063-854_0996ea60-fa2e-0294-e063-6294a90a3f84
    Associated GPIs 36150040200330
    GCN Sequence Number 023382
    GCN Sequence Number Description losartan potassium TABLET 50 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 14851
    HICL Sequence Number 009829
    HICL Sequence Number Description LOSARTAN POTASSIUM
    Brand/Generic Generic
    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 PD-Rx 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 43063-0854-90 (43063085490)

    NDC Package Code 43063-854-90
    Billing NDC 43063085490
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-854-90)
    Marketing Start Date 2018-05-29
    NDC Exclude Flag N
    Pricing Information N/A