Search by Drug Name or NDC

    NDC 70518-3333-00 Bisoprolol Fumarate and Hydrochlorothiazide 2.5; 6.25 mg/1; mg/1 Details

    Bisoprolol Fumarate and Hydrochlorothiazide 2.5; 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 REMEDYREPACK INC.. The primary component is BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 70518-3333
    Product ID 70518-3333_06c1a044-cb6b-be06-e063-6294a90a6687
    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 2.5; 6.25
    Active Ingredient Units mg/1; mg/1
    Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
    Labeler Name REMEDYREPACK 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 ANDA075768
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3333-00 (70518333300)

    NDC Package Code 70518-3333-0
    Billing NDC 70518333300
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3333-0)
    Marketing Start Date 2022-01-13
    NDC Exclude Flag N
    Pricing Information N/A