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    NDC 71335-0595-01 bisoprolol fumarate and hydrochlorothiazide 5; 6.25 mg/1; mg/1 Details

    bisoprolol fumarate and hydrochlorothiazide 5; 6.25 mg/1; mg/1

    bisoprolol fumarate and hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 71335-0595
    Product ID 71335-0595_c8aa01db-b044-462b-af69-bae55087a6a7
    Associated GPIs 36992002130320
    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 bisoprolol fumarate and hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name bisoprolol fumarate and hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5; 6.25
    Active Ingredient Units mg/1; mg/1
    Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079106
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0595-01 (71335059501)

    NDC Package Code 71335-0595-1
    Billing NDC 71335059501
    Package 30 TABLET in 1 BOTTLE, PLASTIC (71335-0595-1)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A