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    NDC 71335-0875-02 telmisartan 80 mg/1 Details

    telmisartan 80 mg/1

    telmisartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is TELMISARTAN.

    Product Information

    NDC 71335-0875
    Product ID 71335-0875_7b7fc5fa-9322-4291-9d75-35a1e81b6b31
    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 80
    Active Ingredient Units mg/1
    Substance Name TELMISARTAN
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203325
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0875-02 (71335087502)

    NDC Package Code 71335-0875-2
    Billing NDC 71335087502
    Package 30 TABLET in 1 BOTTLE (71335-0875-2)
    Marketing Start Date 2019-01-08
    NDC Exclude Flag N
    Pricing Information N/A