Search by Drug Name or NDC

    NDC 71205-0273-30 Hydroxyzine Hydrochloride 25 mg/1 Details

    Hydroxyzine Hydrochloride 25 mg/1

    Hydroxyzine Hydrochloride 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 HYDROXYZINE DIHYDROCHLORIDE.

    Product Information

    NDC 71205-0273
    Product ID 71205-273_7160086d-21ca-4ca0-9aee-1680c2c4d61c
    Associated GPIs 57200040100310
    GCN Sequence Number 003728
    GCN Sequence Number Description hydroxyzine HCl TABLET 25 MG ORAL
    HIC3 Z2P
    HIC3 Description ANTIHISTAMINES - 1ST GENERATION
    GCN 13943
    HICL Sequence Number 001608
    HICL Sequence Number Description HYDROXYZINE HCL
    Brand/Generic Generic
    Proprietary Name Hydroxyzine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydroxyzine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040602
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0273-30 (71205027330)

    NDC Package Code 71205-273-30
    Billing NDC 71205027330
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-273-30)
    Marketing Start Date 2019-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL daefb617-209a-428b-9567-adc5880fa65c Details

    Revised: 11/2022