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    NDC 71205-0207-15 cetirizine hydrochloride 10 mg/1 Details

    cetirizine hydrochloride 10 mg/1

    cetirizine hydrochloride is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is CETIRIZINE HYDROCHLORIDE.

    Product Information

    NDC 71205-0207
    Product ID 71205-207_517ed467-a0d0-43ab-99ce-e6a4808800c4
    Associated GPIs 41550020100320
    GCN Sequence Number 017037
    GCN Sequence Number Description cetirizine HCl TABLET 10 MG ORAL
    HIC3 Z2Q
    HIC3 Description ANTIHISTAMINES - 2ND GENERATION
    GCN 49291
    HICL Sequence Number 006544
    HICL Sequence Number Description CETIRIZINE HCL
    Brand/Generic Generic
    Proprietary Name cetirizine hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Cetirizine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name CETIRIZINE HYDROCHLORIDE
    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 ANDA078336
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0207-15 (71205020715)

    NDC Package Code 71205-207-15
    Billing NDC 71205020715
    Package 15 TABLET in 1 BOTTLE (71205-207-15)
    Marketing Start Date 2019-10-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 198ca875-bb8a-49d5-8809-7121ba119381 Details

    Revised: 4/2022