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    NDC 63629-7854-01 Telmisartan and Hydrochlorothiazide 12.5; 80 mg/1; mg/1 Details

    Telmisartan and Hydrochlorothiazide 12.5; 80 mg/1; mg/1

    Telmisartan 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 HYDROCHLOROTHIAZIDE; TELMISARTAN.

    Product Information

    NDC 63629-7854
    Product ID 63629-7854_c0dd30f3-6c48-455c-a701-72ddeeec93da
    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 Telmisartan and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Telmisartan and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 12.5; 80
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; TELMISARTAN
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203010
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-7854-01 (63629785401)

    NDC Package Code 63629-7854-1
    Billing NDC 63629785401
    Package 30 TABLET in 1 BOTTLE (63629-7854-1)
    Marketing Start Date 2021-12-23
    NDC Exclude Flag N
    Pricing Information N/A