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    NDC 41163-0938-35 levocetirizine dihydrochloride 5 mg/1 Details

    levocetirizine dihydrochloride 5 mg/1

    levocetirizine dihydrochloride is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by United Natural Foods, Inc. dba UNFI. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

    Product Information

    NDC 41163-0938
    Product ID 41163-938_c45a5831-d63d-e0d0-edae-ccdadc661f8a
    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 levocetirizine dihydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name levocetirizine dihydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name LEVOCETIRIZINE DIHYDROCHLORIDE
    Labeler Name United Natural Foods, Inc. dba UNFI
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210375
    Listing Certified Through 2024-12-31

    Package

    NDC 41163-0938-35 (41163093835)

    NDC Package Code 41163-938-35
    Billing NDC 41163093835
    Package 1 BOTTLE in 1 CARTON (41163-938-35) / 35 TABLET, COATED in 1 BOTTLE
    Marketing Start Date 2018-12-31
    NDC Exclude Flag N
    Pricing Information N/A