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    NDC 65162-0292-63 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 Amneal Pharmaceuticals LLC. The primary component is TELMISARTAN.

    Product Information

    NDC 65162-0292
    Product ID 65162-292_af20755d-cc55-4cc2-a7fc-441f5337ff7a
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 Amneal Pharmaceuticals LLC
    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 2024-12-31

    Package

    NDC 65162-0292-63 (65162029263)

    NDC Package Code 65162-292-63
    Billing NDC 65162029263
    Package 3 BLISTER PACK in 1 CARTON (65162-292-63) / 10 TABLET in 1 BLISTER PACK
    Marketing Start Date 2013-05-31
    NDC Exclude Flag N
    Pricing Information N/A