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    NDC 11822-0046-01 Guaifenesin and Pseudoephedrine HCl 600; 60 mg/1; mg/1 Details

    Guaifenesin and Pseudoephedrine HCl 600; 60 mg/1; mg/1

    Guaifenesin and Pseudoephedrine HCl is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid Corporation. The primary component is GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE.

    Product Information

    NDC 11822-0046
    Product ID 11822-0046_df73a993-2189-a555-4670-bc9ee7ea63e2
    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 Guaifenesin and Pseudoephedrine HCl
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin and Pseudoephedrine HCL
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 600; 60
    Active Ingredient Units mg/1; mg/1
    Substance Name GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
    Labeler Name Rite Aid Corporation
    Pharmaceutical Class Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208369
    Listing Certified Through 2024-12-31

    Package

    NDC 11822-0046-01 (11822004601)

    NDC Package Code 11822-0046-1
    Billing NDC 11822004601
    Package 1 BLISTER PACK in 1 CARTON (11822-0046-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2022-02-01
    NDC Exclude Flag N
    Pricing Information N/A