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    NDC 72789-0023-30 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 PD-Rx Pharmaceuticals, Inc.. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

    Product Information

    NDC 72789-0023
    Product ID 72789-023_05f98f21-12f7-5d8e-e063-6294a90a2681
    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 PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091264
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0023-30 (72789002330)

    NDC Package Code 72789-023-30
    Billing NDC 72789002330
    Package 30 TABLET in 1 BOTTLE, PLASTIC (72789-023-30)
    Marketing Start Date 2019-10-17
    NDC Exclude Flag N
    Pricing Information N/A