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    NDC 43547-0442-09 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 Solco Healthcare LLC. The primary component is HYDROCHLOROTHIAZIDE; TELMISARTAN.

    Product Information

    NDC 43547-0442
    Product ID 43547-442_a0a83c79-b565-4c82-a127-5e87816cbaef
    Associated GPIs 36994002600340
    GCN Sequence Number 047324
    GCN Sequence Number Description telmisartan/hydrochlorothiazid TABLET 80-12.5MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 12259
    HICL Sequence Number 021873
    HICL Sequence Number Description TELMISARTAN/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    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 Solco Healthcare LLC
    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 ANDA209028
    Listing Certified Through 2024-12-31

    Package

    NDC 43547-0442-09 (43547044209)

    NDC Package Code 43547-442-09
    Billing NDC 43547044209
    Package 90 TABLET in 1 BOTTLE (43547-442-09)
    Marketing Start Date 2018-02-05
    NDC Exclude Flag N
    Pricing Information N/A