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    NDC 51285-0040-01 Ziac 10; 6.25 mg/1; mg/1 Details

    Ziac 10; 6.25 mg/1; mg/1

    Ziac is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Women's Health LLC. The primary component is BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 51285-0040
    Product ID 51285-040_5bf77f2f-a676-4eee-927d-e0a7fad342a0
    Associated GPIs 36992002130330
    GCN Sequence Number 021141
    GCN Sequence Number Description bisoprolol/hydrochlorothiazide TABLET 10-6.25MG ORAL
    HIC3 J7H
    HIC3 Description BETA-BLOCKERS AND THIAZIDE,THIAZIDE-LIKE DIURETICS
    GCN 45063
    HICL Sequence Number 008715
    HICL Sequence Number Description BISOPROLOL FUMARATE/HYDROCHLOROTHIAZIDE
    Brand/Generic Brand
    Proprietary Name Ziac
    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 10; 6.25
    Active Ingredient Units mg/1; mg/1
    Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
    Labeler Name Teva Women's Health LLC
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020186
    Listing Certified Through n/a

    Package

    NDC 51285-0040-01 (51285004001)

    NDC Package Code 51285-040-01
    Billing NDC 51285004001
    Package 30 TABLET, FILM COATED in 1 BOTTLE (51285-040-01)
    Marketing Start Date 1993-10-26
    NDC Exclude Flag N
    Pricing Information N/A