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    NDC 62756-0368-08 Metoprolol Tartrate and Hydrochlorothiazide 25; 100 mg/1; mg/1 Details

    Metoprolol Tartrate and Hydrochlorothiazide 25; 100 mg/1; mg/1

    Metoprolol Tartrate and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE.

    Product Information

    NDC 62756-0368
    Product ID 62756-368_09b3341a-4a9b-4db9-94b5-b74c034f409d
    Associated GPIs
    GCN Sequence Number 000412
    GCN Sequence Number Description metoprolol/hydrochlorothiazide TABLET 100MG-25MG ORAL
    HIC3 J7H
    HIC3 Description BETA-BLOCKERS AND THIAZIDE,THIAZIDE-LIKE DIURETICS
    GCN 51551
    HICL Sequence Number 000143
    HICL Sequence Number Description METOPROLOL TARTRATE/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Metoprolol Tartrate and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metoprolol Tartrate and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
    Labeler Name Sun Pharmaceutical Industries, 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 ANDA090654
    Listing Certified Through 2024-12-31

    Package

    NDC 62756-0368-08 (62756036808)

    NDC Package Code 62756-368-08
    Billing NDC 62756036808
    Package 100 TABLET in 1 BOTTLE (62756-368-08)
    Marketing Start Date 2022-04-01
    NDC Exclude Flag N
    Pricing Information N/A