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    NDC 13668-0159-01 telmisartan and hydrochlorthiazide 12.5; 40 mg/1; mg/1 Details

    telmisartan and hydrochlorthiazide 12.5; 40 mg/1; mg/1

    telmisartan and hydrochlorthiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is HYDROCHLOROTHIAZIDE; TELMISARTAN.

    Product Information

    NDC 13668-0159
    Product ID 13668-159_dafab77d-e949-759f-e053-2a95a90a5f8a
    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 hydrochlorthiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name telmisartan and hydrochlorthiazide
    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 Torrent Pharmaceuticals Limited
    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 ANDA201192
    Listing Certified Through 2023-12-31

    Package

    NDC 13668-0159-01 (13668015901)

    NDC Package Code 13668-159-01
    Billing NDC 13668015901
    Package 100 TABLET in 1 BOTTLE (13668-159-01)
    Marketing Start Date 2014-02-25
    NDC Exclude Flag N
    Pricing Information N/A