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    NDC 33342-0117-51 Candesartan 32 mg/1 Details

    Candesartan 32 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 33342-0117
    Product ID 33342-117_4079c843-42ee-4f7a-a4a0-9498ba6cf12d
    Associated GPIs 36150020100340
    GCN Sequence Number 040659
    GCN Sequence Number Description candesartan cilexetil TABLET 32 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 73545
    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 32
    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 33342-0117-51 (33342011751)

    NDC Package Code 33342-117-51
    Billing NDC 33342011751
    Package 300 TABLET in 1 CONTAINER (33342-117-51)
    Marketing Start Date 2016-12-06
    NDC Exclude Flag N
    Pricing Information N/A