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    NDC 71205-0210-30 Levocetirizine Dihydrochloride 5 mg/1 Details

    Levocetirizine Dihydrochloride 5 mg/1

    Levocetirizine Dihydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

    Product Information

    NDC 71205-0210
    Product ID 71205-210_1913d2a6-6558-4d2b-bc1e-54cdef6623eb
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name LEVOCETIRIZINE DIHYDROCHLORIDE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202046
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0210-30 (71205021030)

    NDC Package Code 71205-210-30
    Billing NDC 71205021030
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)
    Marketing Start Date 2019-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL f10cfe9a-1884-4a65-b827-8fd781fb75c4 Details

    Revised: 1/2020