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    NDC 33342-0115-51 Candesartan 8 mg/1 Details

    Candesartan 8 mg/1

    Candesartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Macleods Pharmaceuticals Limited. The primary component is CANDESARTAN CILEXETIL.

    Product Information

    NDC 33342-0115
    Product ID 33342-115_4079c843-42ee-4f7a-a4a0-9498ba6cf12d
    Associated GPIs 36150020100320
    GCN Sequence Number 037016
    GCN Sequence Number Description candesartan cilexetil TABLET 8 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 73543
    HICL Sequence Number 016913
    HICL Sequence Number Description CANDESARTAN CILEXETIL
    Brand/Generic Generic
    Proprietary Name Candesartan
    Proprietary Name Suffix n/a
    Non-Proprietary Name Candesartan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 8
    Active Ingredient Units mg/1
    Substance Name CANDESARTAN CILEXETIL
    Labeler Name Macleods Pharmaceuticals Limited
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203813
    Listing Certified Through 2024-12-31

    Package

    NDC 33342-0115-51 (33342011551)

    NDC Package Code 33342-115-51
    Billing NDC 33342011551
    Package 300 TABLET in 1 CONTAINER (33342-115-51)
    Marketing Start Date 2016-12-06
    NDC Exclude Flag N
    Pricing Information N/A