Search by Drug Name or NDC

    NDC 00573-2660-24 ALAVERT ALLERGY SINUS D-12 5; 120 mg/1; mg/1 Details

    ALAVERT ALLERGY SINUS D-12 5; 120 mg/1; mg/1

    ALAVERT ALLERGY SINUS D-12 is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is LORATADINE; PSEUDOEPHEDRINE SULFATE.

    Product Information

    NDC 00573-2660
    Product ID 0573-2660_60d4d282-c9fb-4d77-b832-80d9d4841eec
    Associated GPIs 43993002597430
    GCN Sequence Number 017181
    GCN Sequence Number Description loratadine/pseudoephedrine TAB ER 12H 5 MG-120MG ORAL
    HIC3 Z2O
    HIC3 Description 2ND GEN ANTIHISTAMINE AND DECONGESTANT COMBINATION
    GCN 63570
    HICL Sequence Number 006605
    HICL Sequence Number Description LORATADINE/PSEUDOEPHEDRINE SULFATE
    Brand/Generic Brand
    Proprietary Name ALAVERT ALLERGY SINUS D-12
    Proprietary Name Suffix n/a
    Non-Proprietary Name loratadine, pseudoephedrine sulfate
    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 LORATADINE; PSEUDOEPHEDRINE SULFATE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076050
    Listing Certified Through 2024-12-31

    Package

    NDC 00573-2660-24 (00573266024)

    NDC Package Code 0573-2660-24
    Billing NDC 00573266024
    Package 4 BLISTER PACK in 1 CARTON (0573-2660-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2004-01-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b6c03018-9338-9789-bcdb-2eb91aac8021 Details

    Revised: 11/2020