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    NDC 00363-0989-12 Wal-Zyr D 5; 120 mg/1; mg/1 Details

    Wal-Zyr D 5; 120 mg/1; mg/1

    Wal-Zyr D is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE.

    Product Information

    NDC 00363-0989
    Product ID 0363-0989_cefefe10-2f8d-4e93-a525-b4ea59f81ffb
    Associated GPIs
    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 Wal-Zyr D
    Proprietary Name Suffix n/a
    Non-Proprietary Name Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 5; 120
    Active Ingredient Units mg/1; mg/1
    Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
    Labeler Name Walgreen Company
    Pharmaceutical Class Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090922
    Listing Certified Through 2024-12-31

    Package

    NDC 00363-0989-12 (00363098912)

    NDC Package Code 0363-0989-12
    Billing NDC 00363098912
    Package 2 BLISTER PACK in 1 CARTON (0363-0989-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2018-11-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 778ba62e-6cce-4d0f-b6d9-48b35ef40da7 Details

    Revised: 10/2022