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    NDC 63868-0473-35 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 Chain Drug Marketing Association INC. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

    Product Information

    NDC 63868-0473
    Product ID 63868-473_3c8bb96b-e283-d8dc-b1ec-6590a3feb121
    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 Chain Drug Marketing Association INC
    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 63868-0473-35 (63868047335)

    NDC Package Code 63868-473-35
    Billing NDC 63868047335
    Package 1 BOTTLE in 1 CARTON (63868-473-35) / 35 TABLET, COATED in 1 BOTTLE
    Marketing Start Date 2020-06-24
    NDC Exclude Flag N
    Pricing Information N/A