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    NDC 42291-0790-30 Telmisartan 20 mg/1 Details

    Telmisartan 20 mg/1

    Telmisartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is TELMISARTAN.

    Product Information

    NDC 42291-0790
    Product ID 42291-790_0e9ac170-4a2f-d07c-e063-6394a90af8f4
    Associated GPIs 36150070000310
    GCN Sequence Number 047126
    GCN Sequence Number Description telmisartan TABLET 20 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 23833
    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 20
    Active Ingredient Units mg/1
    Substance Name TELMISARTAN
    Labeler Name AvKARE
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204415
    Listing Certified Through 2025-12-31

    Package

    NDC 42291-0790-30 (42291079030)

    NDC Package Code 42291-790-30
    Billing NDC 42291079030
    Package 30 TABLET in 1 BOTTLE (42291-790-30)
    Marketing Start Date 2017-12-20
    NDC Exclude Flag N
    Pricing Information N/A