Search by Drug Name or NDC

    NDC 10135-0734-01 ATENOLOL AND CHLORTHALIDONE 100; 25 mg/1; mg/1 Details

    ATENOLOL AND CHLORTHALIDONE 100; 25 mg/1; mg/1

    ATENOLOL AND CHLORTHALIDONE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by MARLEX PHARMACEUTICALS, INC. The primary component is ATENOLOL; CHLORTHALIDONE.

    Product Information

    NDC 10135-0734
    Product ID 10135-734_f5647029-c7b7-355c-e053-2995a90acb85
    Associated GPIs 36992002100320
    GCN Sequence Number 000419
    GCN Sequence Number Description atenolol/chlorthalidone TABLET 100MG-25MG ORAL
    HIC3 J7H
    HIC3 Description BETA-BLOCKERS AND THIAZIDE,THIAZIDE-LIKE DIURETICS
    GCN 66991
    HICL Sequence Number 000147
    HICL Sequence Number Description ATENOLOL/CHLORTHALIDONE
    Brand/Generic Generic
    Proprietary Name ATENOLOL AND CHLORTHALIDONE
    Proprietary Name Suffix n/a
    Non-Proprietary Name atenolol and chlorthalidone tablet
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 100; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name ATENOLOL; CHLORTHALIDONE
    Labeler Name MARLEX PHARMACEUTICALS, INC
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215560
    Listing Certified Through 2024-12-31

    Package

    NDC 10135-0734-01 (10135073401)

    NDC Package Code 10135-734-01
    Billing NDC 10135073401
    Package 100 TABLET in 1 BOTTLE (10135-734-01)
    Marketing Start Date 2022-03-01
    NDC Exclude Flag N
    Pricing Information N/A