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    NDC 68180-0193-09 Telmisartan and Hydrochlorothiazide 12.5; 40 mg/1; mg/1 Details

    Telmisartan and Hydrochlorothiazide 12.5; 40 mg/1; mg/1

    Telmisartan and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE; TELMISARTAN.

    Product Information

    NDC 68180-0193
    Product ID 68180-193_f43ef4e7-e34c-40c7-b776-2381db92162f
    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 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; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; TELMISARTAN
    Labeler Name Lupin 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 ANDA
    Application Number ANDA091351
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0193-09 (68180019309)

    NDC Package Code 68180-193-09
    Billing NDC 68180019309
    Package 90 TABLET in 1 BOTTLE (68180-193-09)
    Marketing Start Date 2014-08-07
    NDC Exclude Flag N
    Pricing Information N/A