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    NDC 67877-0483-90 telmisartan 40 mg/1 Details

    telmisartan 40 mg/1

    telmisartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is TELMISARTAN.

    Product Information

    NDC 67877-0483
    Product ID 67877-483_f10918d7-d964-5c11-e053-2a95a90af1a4
    Associated GPIs 36150070000320
    GCN Sequence Number 040910
    GCN Sequence Number Description telmisartan TABLET 40 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 23831
    HICL Sequence Number 018839
    HICL Sequence Number Description TELMISARTAN
    Brand/Generic Generic
    Proprietary Name telmisartan
    Proprietary Name Suffix n/a
    Non-Proprietary Name telmisartan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name TELMISARTAN
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205150
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0483-90 (67877048390)

    NDC Package Code 67877-483-90
    Billing NDC 67877048390
    Package 90 TABLET in 1 BOTTLE (67877-483-90)
    Marketing Start Date 2019-07-25
    NDC Exclude Flag N
    Pricing Information N/A