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    NDC 68788-7934-06 levocetirizine dihydrochloride 5 mg/1 Details

    levocetirizine dihydrochloride 5 mg/1

    levocetirizine dihydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

    Product Information

    NDC 68788-7934
    Product ID 68788-7934_e09ab3c1-d858-43d3-938c-ccb18b9c5043
    Associated GPIs 41550027100320
    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 PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name LEVOCETIRIZINE DIHYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203646
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7934-06 (68788793406)

    NDC Package Code 68788-7934-6
    Billing NDC 68788793406
    Package 60 TABLET in 1 BOTTLE (68788-7934-6)
    Marketing Start Date 2021-06-15
    NDC Exclude Flag N
    Pricing Information N/A