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    NDC 71335-1841-02 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 Bryant Ranch Prepack. The primary component is TELMISARTAN.

    Product Information

    NDC 71335-1841
    Product ID 71335-1841_81c2ee77-f3ce-4366-a609-457442509457
    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 Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207016
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1841-02 (71335184102)

    NDC Package Code 71335-1841-2
    Billing NDC 71335184102
    Package 90 TABLET in 1 BOTTLE (71335-1841-2)
    Marketing Start Date 2022-02-14
    NDC Exclude Flag N
    Pricing Information N/A