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    NDC 72578-0114-06 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, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Viona Pharmaceuticals Inc. The primary component is BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 72578-0114
    Product ID 72578-114_550e6ac5-3ece-461f-a9c5-2e4050a5eabb
    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 Bisoprolol Fumarate and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name bisoprolol fumarate and hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 6.25
    Active Ingredient Units mg/1; mg/1
    Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
    Labeler Name Viona Pharmaceuticals Inc
    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 ANDA215666
    Listing Certified Through 2025-12-31

    Package

    NDC 72578-0114-06 (72578011406)

    NDC Package Code 72578-114-06
    Billing NDC 72578011406
    Package 30 TABLET, FILM COATED in 1 BOTTLE (72578-114-06)
    Marketing Start Date 2023-03-01
    NDC Exclude Flag N
    Pricing Information N/A