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    NDC 00597-0043-37 Micardis HCT 12.5; 40 mg/1; mg/1 Details

    Micardis HCT 12.5; 40 mg/1; mg/1

    Micardis HCT is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Boehringer Ingelheim Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE; TELMISARTAN.

    Product Information

    NDC 00597-0043
    Product ID 0597-0043_c58fc0c9-d4dc-4fc5-9cb5-bfd7f6fe5636
    Associated GPIs 36994002600320
    GCN Sequence Number 047326
    GCN Sequence Number Description telmisartan/hydrochlorothiazid TABLET 40-12.5 MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 12257
    HICL Sequence Number 021873
    HICL Sequence Number Description TELMISARTAN/HYDROCHLOROTHIAZIDE
    Brand/Generic Brand
    Proprietary Name Micardis HCT
    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; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; TELMISARTAN
    Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
    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 NDA
    Application Number NDA021162
    Listing Certified Through 2024-12-31

    Package

    NDC 00597-0043-37 (00597004337)

    NDC Package Code 0597-0043-37
    Billing NDC 00597004337
    Package 3 BLISTER PACK in 1 CARTON (0597-0043-37) / 10 TABLET in 1 BLISTER PACK
    Marketing Start Date 2000-12-01
    NDC Exclude Flag N
    Pricing Information N/A